| Name |
Description |
Abstract |
Status |
Publication date |
Edition |
Number of pages |
Technical committee |
ICS |
| ISO 15927-1:2003 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 1: Monthly means of single meteorological elements |
ISO 15927-1:2003 specifies procedures for calculating and presenting the monthly means of those parameters of climatic data needed to assess some aspects of the thermal and moisture performance of buildings. Numerical values for any locations should be obtained from the meteorological service in the relevant country.
ISO 15927-1:2003 covers the following single climate variables: air temperature; atmospheric humidity; wind speed; precipitation; solar radiation; longwave radiation.
Meteorological instrumentation and methods of observation are not covered; these are specified by the World Meteorological Organisation (WMO).
|
Published |
2003-11 |
Edition : 1 |
Number of pages : 26 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 15927-2:2009 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 2: Hourly data for design cooling load |
ISO 15927-2:2009 gives the definition, and specifies methods of calculation and presentation of the monthly external design climate to be used in determining the design cooling load of buildings and the design of air conditioning systems.
|
Published |
2009-02 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 15927-3:2009 |
Hygrothermal performance of buildings - Calculation and presentation of climatic data — Part 3: Calculation of a driving rain index for vertical surfaces from hourly wind and rain data |
ISO 15927-3:2009 specifies two procedures for providing an estimate of the quantity of water likely to impact on a wall of any given orientation. It takes account of topography, local sheltering and the type of building and wall.
The first method, based on coincident hourly rainfall and wind data, defines the method of calculation of the annual average index, which influences the moisture content of an absorbent surface, such as masonry, and the spell index, which influences the likelihood of rain penetration through masonry and joints in other walling systems.
The second method, based on average wind data and a qualitative recording of the presence and intensity of rain (the present weather code for rain), defines a method for calculating the spell length during which an absorbent material such as masonry is moistened, having a 10 % probability of being exceeded in any year (commonly referred to as having a mean return period of 10 years).
ISO 15927-3:2009 provides a comparison between the two methods.
ISO 15927-3:2009 gives procedures to correct the results of both methods for topography, local sheltering and the type of building and wall.
The methods included in ISO 15927-3:2009 do not apply in mountainous areas with sheer cliffs or deep gorges, in areas in which more than 25 % of the annual rainfall comes from severe convective storms, and in areas and during periods when a significant proportion of precipitation is made up of snow or hail.
|
Published |
2009-03 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 16622:2002 |
Meteorology — Sonic anemometers/thermometers — Acceptance test methods for mean wind measurements |
ISO 16622:2002 defines test methods of the performance of sonic anemometers/thermometers which employ the inverse time measurement for velocity of sound along differently oriented paths. It is applicable to designs measuring two or three components of the wind vector within an unlimited (360°) azimuthal acceptance angle.
|
Published |
2002-09 |
Edition : 1 |
Number of pages : 21 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 15927-4:2005 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 4: Hourly data for assessing the annual energy use for heating and cooling |
ISO 15927-4:2005 specifies a method for constructing a reference year of hourly values of appropriate meteorological data suitable for assessing the average annual energy for heating and cooling. Other reference years representing average conditions can be constructed for special purposes. The procedures in this part of ISO 15927-4:2005 are not suitable for constructing extreme or semi-extreme years for simulation of, for example, moisture damage or energy demand in cold years.
Meteorological instrumentation and methods of observation are not covered.
|
Published |
2005-07 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 15927-5:2004 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 5: Data for design heat load for space heating |
ISO 15927-5:2004 specifies the definition, method of calculation and method of presentation of the climatic data to be used in determining the design heat load for space heating in buildings. These include the winter external design air temperatures and the relevant wind speed and direction, where appropriate.
Heat loss through the ground, which also contributes to the heat load for buildings, depends on longer-term temperature changes; methods for calculating ground heat loss are given in ISO 13370.
|
Published |
2004-11 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 15927-5:2004/Amd 1:2011 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 5: Data for design heat load for space heating — Amendment 1 |
|
Published |
2011-11 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 15927-6:2007 |
Hygrothermal performance of buildings — Calculation and presentation of climatic data — Part 6: Accumulated temperature differences (degree-days) |
ISO 15927-6:2007 specifies the definition, method of computation and method of presentation of data on accumulated temperature differences, used for assessing the energy used for space heating in buildings. These are normally expressed in degree‑hours or degree-days, and such data are often referred to simply as "heating degree-hours" or "heating degree-days".
ISO 15927-6:2007 includes approximate methods for calculating accumulated temperature differences based on hourly or daily mean temperatures and for estimating monthly values to any base temperature, for use when data computed directly from meteorological air temperature records are not available.
In some countries, a threshold temperature different from the base temperature is used. ISO 15927-6:2007 does not cover this.
|
Published |
2007-09 |
Edition : 1 |
Number of pages : 13 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
91.120.10
Thermal insulation of buildings
|
| ISO 16457:2014 |
Space systems — Space environment (natural and artificial) — The Earth's ionosphere model: international reference ionosphere (IRI) model and extensions to the plasmasphere |
ISO 16457:2014 provides guidance to potential users for the specification of the global distribution of ionosphere densities and temperatures, as well as the total content of electrons in the height interval from 50 km to 1 500 km. It includes and explains several options for a plasmaspheric extension of the model, embracing the geographical area between latitudes of 80°S and 80°N and longitudes of 0°E to 360°E, for any time of day, any day of year, and various solar and magnetic activity conditions.
|
Withdrawn |
2014-04 |
Edition : 1 |
Number of pages : 15 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
49.140
Space systems and operations
|
| ISO/TS 16457:2009 |
Space systems — Space environment (natural and artificial) — The Earth's ionosphere model: international reference ionosphere (IRI) model and extensions to the plasmasphere |
ISO/TS 16457:2009 provides guidance to potential users for the specification of the global distribution of ionosphere densities and temperatures, as well as the total content of electrons in the height interval from 50 km to 1 500 km. It includes and explains several options for a plasmaspheric extension of the model, embracing the geographical area between latitudes of 80°S and 80°N and longitudes of 0°E to 360°E, for any time of day, any day of year, and various solar and magnetic activity conditions.
|
Withdrawn |
2009-02 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
49.140
Space systems and operations
|
| ISO 16457:2022 |
Space environment (natural and artificial) — The Earth's ionosphere model — International reference ionosphere (IRI) model and extensions to the plasmasphere |
This document provides guidance to potential users for the specification of the global distribution of ionosphere densities and temperatures, as well as the total content of electrons in the height interval from 50 km to 1 500 km. It includes and explains several options for a plasmaspheric extension of the model, embracing the geographical area between latitudes of 80°S and 80°N and longitudes of 0°E to 360°E, for any time of day, any day of year, and various solar and magnetic activity conditions.
A brief introduction to ionospheric and plasmaspheric physics is given in Annex A. Annex B provides an overview over physical models, because they are important for understanding and modelling the physical processes that produce the ionospheric plasma.
|
Published |
2022-02 |
Edition : 2 |
Number of pages : 19 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
49.140
Space systems and operations
|
| ISO 17713-1:2007 |
Meteorology — Wind measurements — Part 1: Wind tunnel test methods for rotating anemometer performance |
ISO 17713-1:2007 describes wind tunnel test methods for determining performance characteristics of rotating anemometers, specifically cup anemometers and propeller anemometers. It also describes an acceptance test and unambiguous methods for measuring the starting threshold, distance constant, transfer function and off-axis response of a rotating anemometer in a wind tunnel.
|
Published |
2007-05 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
17.080
Measurement of time, velocity, acceleration, angular velocity
|
| ISO 17714:2007 |
Meteorology — Air temperature measurements — Test methods for comparing the performance of thermometer shields/screens and defining important characteristics |
ISO 17714:2007 defines characteristics of a thermometer shield/screen. It also defines test methods to inter-compare the behaviour of different screen designs.
Although screens are usually used for both air temperature and humidity measurements, ISO 17714:2007 is applicable only to temperature measurements.
Both naturally and artificially ventilated screens are considered.
|
Published |
2007-07 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
17.200.20
Temperature-measuring instruments
|
| ISO 17717:2017 |
Meteorological balloons — Specification |
ISO 17717:2017 specifies the minimum requirements and test methods for meteorological balloons made from natural rubber latex or natural rubber latex compounded with synthetic rubber emulsion.
ISO 17717:2017 applies to two types of balloon:
- Type 1: meteorological balloon produced by dipping process;
- Type 2: meteorological balloon produced by moulding process.
|
Published |
2017-08 |
Edition : 1 |
Number of pages : 21 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
83.140.99
Other rubber and plastics products
|
| ISO/DIS 17717 |
Meteorological balloons — Specification |
ISO 17717:2017 specifies the minimum requirements and test methods for meteorological balloons made from natural rubber latex or natural rubber latex compounded with synthetic rubber emulsion.
ISO 17717:2017 applies to two types of balloon:
- Type 1: meteorological balloon produced by dipping process;
- Type 2: meteorological balloon produced by moulding process.
|
Under development |
|
Edition : 2 |
Number of pages : 21 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
83.140.99
Other rubber and plastics products
|
| ISO 19289:2015 |
Air quality — Meteorology — Siting classifications for surface observing stations on land |
ISO 19289:2015 indicates exposure rules for various sensors, but what should be done when these conditions are not fulfilled? There are sites that do not respect the recommended exposure rules. Consequently, a classification has been established to help determine the given site's representativeness on a small scale (impact of the surrounding environment).
The classification process helps the actors and managers of a network to better take into consideration the exposure rules and thus it often improves the siting. At least, the siting environment is known and documented in the metadata. It is obviously possible and recommended to fully document the site but the risk is that a fully documented site might increase the complexity of the metadata, which would often restrict their operational use. That is why this siting classification is defined to condense the information and facilitate the operational use of this metadata information.
A site as a whole has no single classification number. Each parameter being measured at a site has its own class and is sometimes different from the others. If a global classification of a site is required, the maximum value of the parameters' classes can be used.
In ISO 19289:2015, the classification is (occasionally) completed with an estimated uncertainty due to siting, which has to be added in the uncertainty budget of the measurement. This estimation is coming from bibliographic studies and/or some comparative tests.
The primary objective of this classification is to document the presence of obstacles close to the measurement site.
|
Published |
2015-03 |
Edition : 1 |
Number of pages : 14 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 19926-1:2019 |
Meteorology — Weather radar — Part 1: System performance and operation |
ISO 19926-1:2019 specifies system performance of ground-based weather radar systems measuring the atmosphere using frequencies between 2 GHz and 10 GHz. These systems are suitable for the area-wide detection of precipitation and other meteorological targets at different altitudes. This document also describes ways to verify the different aspects of system performance, including infrastructure.
ISO 19926-1:2019 is applicable to linear polarization parabolic radar systems, dual-polarization and single-polarization radars. It does not apply to fan-beam radars [narrow in azimuth (AZ) and broad in elevation (EL)], including marine and aeronautical surveillance radars, which are used for, but are not primarily designed for, weather applications. Phased-array radars with electronically formed and steered beams, including multi-beam, with non-circular off-bore sight patterns, are new and insufficient performance information is available.
ISO 19926-1:2019 does not describe weather radar technology and its applications. Weather radar systems can be used for applications such as quantitative precipitation estimation (QPE), the classification of hydrometeors (e.g. hail), the estimation of wind speeds and the detection and surveillance of severe meteorological phenomena (e.g. microburst, tornado). Some of these applications have particular requirements for the positioning of the radar system or need specific measurement strategies. However, the procedures for calibration and maintenance described in this document apply here as well.
ISO 19926-1:2019 addresses manufacturers and radar operators.
|
Published |
2019-02 |
Edition : 1 |
Number of pages : 93 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 21413:2005 |
Manual methods for the measurement of a groundwater level in a well |
ISO 21413:2005 develops procedures and prescribes the minimum accuracy required of water-level measurements made in wells using graduated steel tapes, electric tapes and air lines. Procedures and accuracy requirements for measuring water levels in a flowing well are also included, as are procedures required to establish a permanent measuring point. ISO 21413:2005 discusses the advantages and limitations of each method and requirements for recording the data. ISO 21413:2005 does not include methods that use automated electrical or mechanical means to measure and record water levels.
|
Published |
2005-10 |
Edition : 1 |
Number of pages : 30 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
17.060
Measurement of volume, mass, density, viscosity
|
| ISO/TR 21414:2016 |
Hydrometry — Groundwater — Surface geophysical surveys for hydrogeological purposes |
The application of geophysical methods is an evolving science that can address a variety of objectives in groundwater investigations. However, because the successful application of geophysical methods depends on the available technology, logistics, and expertise of the investigator, there can be no single set of field procedures or approaches prescribed for all cases. ISO/TR 21414:2016 provides guidelines that are useful for conducting geophysical surveys for a variety of objectives (including environmental aspects), within the limits of modern-day instrumentation and interpretive techniques, are provided. The more commonly used field techniques and practices are described, with an emphasis on electrical resistivity, electromagnetic, and seismic refraction techniques as these are widely used in groundwater exploration. Theoretical aspects and details of interpretational procedures are referred to only in a general way. For full details, reference is intended to be made to specialized texts listed in the Bibliography.
|
Published |
2016-02 |
Edition : 1 |
Number of pages : 55 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 23032:2022 |
Meteorology — Ground-based remote sensing of wind — Radar wind profiler |
This document provides guidelines for the design, manufacture, installation, and maintenance of a WPR. It describes the following:
— Measurement principle (Clause 5). Scatterers that produce echoes and methods of wind velocity measurement are described. The description of the measurement principle mainly aims at providing the information necessary for describing the guidelines in Clauses 6 to 11.
— Guidelines for WPR system (Clause 6). Frequency, hardware, software, and signal processing are described. They are mainly applied in designing and manufacturing the hardware and software of WPR.
— Guidelines for system performance (Clause 7). Measurement resolution, range sampling, radar sensitivity evaluation, and measurement accuracy are described. They can be used for estimating the measurement performance of a WPR’s system design and operation.
— Guidelines for quality control (QC) in digital signal processing (Clause 8).
— Guidelines for measurement products and data format (Clause 9). Measurement products obtained by a WPR and their data levels are defined. Guidelines for data file formats are also described.
— Guidelines for installation (Clause 10) and maintenance (Clause 11).
This document does not aim at providing a thorough description of the measurement principle, WPR systems, and WPR applications. For further details of these items, users are referred to technical books (e.g. References [1],[2],[3]).
WPRs are referred to by various names (e.g. radar wind profiler, wind profiler radar, wind profiling radar, atmospheric radar, or clear-air Doppler radar). Conventional naming for WPRs should be allowed.
|
Published |
2022-12 |
Edition : 1 |
Number of pages : 95 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO/TR 23211:2009 |
Hydrometry — Measuring the water level in a well using automated pressure transducer methods |
ISO/TR 23211:2009 provides information about the functional requirements of instrumentation for measuring the water level in a well using automated pressure transducer methods.
ISO/TR 23211:2009 provides guidance for the proper selection, installation and operation of submersible pressure transducers and data loggers for the collection of hydrologic data, primarily for the collection of water-level data from wells. Basic principles, measurement needs and considerations for operating submersible pressure transducers are described and the systematic errors inherent in their use are discussed. Standard operational procedures for data collection and data processing, as well as applications of transducers for specific types of hydrologic investigations are included. Basic concepts regarding the physics of pressure and the mechanics of measuring pressure are presented, along with information on the electronics used to make and record these measurements. Guidelines for transducer calibration, proper use and quality assurance of data also are presented. Ground water field applications of pressure transducer systems are discussed, as are common problems that may corrupt data, along with suggestions for field repairs.
An informative annex provides guidance on the types of pressure transducers commonly used for water-level measurement and the measurement uncertainty associated with them.
|
Published |
2009-07 |
Edition : 1 |
Number of pages : 59 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 23435:2022 |
Air quality — Test methods for snow depth sensors |
This document provides requirements for the evaluation and use of test method for snow depth sensors. This document is applicable to the following types of automatic snow depth sensors which employ different ranging technologies by which the sensors measure the distance from the snow surface to the sensor:
a) Ultrasonic type, also known as sonic ranging depth sensors;
b) Optical laser snow depth sensors including single point and multipoint snow depth sensors;
c) Other snow depth sensors.
This document mainly covers two major tests: a laboratory(indoor) test and a field (outdoor) test. The laboratory test includes the basic performance test and other tests under various environmental changes. The field test is proposed to ensure the performance of the snow depth sensors in field measurement conditions. For the field test, both the natural ground and artificial target surface such as snow plates are considered for the procedures defined in this document.
|
Published |
2022-04 |
Edition : 1 |
Number of pages : 15 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 28902-1:2012 |
Air quality — Environmental meteorology — Part 1: Ground-based remote sensing of visual range by lidar |
This part of ISO 28902 mainly specifies the requirements in order to perform visual range lidar measurements
for the determination of direction-dependent meteorological optical range (MOR). The term "visual-range lidar"
is used in this part of ISO 28902 to apply to the lidar systems making visual-range measurements, commonly
referred to as "visibility measurements". Due to physical approximations, quantitative determination is limited
to a meteorological optical range of between 30 m and 2 000 m. For this range, this part of ISO 28902
specifies the performance of visual-range lidar systems utilizing the method of range‑integrated visual-range
measurements based on light extinction. The following parameters can be calculated based on the directiondependent
meteorological optical range:
a) horizontal visual range;
b) vertical visual range;
c) slant visual range.
NOTE The measures for visibility are strongly related to the historical definitions of visibility, which are related to human
observers. The lidar technique extends the definitions to various conditions, such as daylight and night-time conditions.
In addition, this measurement principle enables the user to retrieve information on cloud base height, boundary
layer depth, fog banks and aerosol profiles due to the signal attenuation by water vapour and/or aerosols.
Examples of these applications are given in Annex C.
This part of ISO 28902 can be applied in the following areas:
— meteorological stations;
— airports;
— harbours;
— waterways;
— roads and motorways;
— automotive;
— oil platforms.
|
Published |
2012-01 |
Edition : 1 |
Number of pages : 30 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
;
13.040.99
Other standards related to air quality
|
| ISO 15558:1998 |
Practice for use of a polymethylmethacrylate dosimetry system |
|
Withdrawn |
1998-12 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
17.240
Radiation measurements
|
| ISO 28902-2:2017 |
Air quality — Environmental meteorology — Part 2: Ground-based remote sensing of wind by heterodyne pulsed Doppler lidar |
ISO 28902-2:2017 specifies the requirements and performance test procedures for heterodyne pulsed Doppler lidar techniques and presents their advantages and limitations. The term "Doppler lidar" used in this document applies solely to heterodyne pulsed lidar systems retrieving wind measurements from the scattering of laser light onto aerosols in the atmosphere. A description of performances and limits are described based on standard atmospheric conditions.
This document describes the determination of the line-of-sight wind velocity (radial wind velocity).
NOTE Derivation of wind vector from individual line-of-sight measurements is not described in this document since it is highly specific to a particular wind lidar configuration. One example of the retrieval of the wind vector can be found in Annex B.
ISO 28902-2:2017 does not address the retrieval of the wind vector.
ISO 28902-2:2017 may be used for the following application areas:
- meteorological briefing for, e.g. aviation, airport safety, marine applications and oil platforms;
- wind power production, e.g. site assessment and power curve determination;
- routine measurements of wind profiles at meteorological stations;
- air pollution dispersion monitoring;
- industrial risk management (direct data monitoring or by assimilation into micro-scale flow models);
- exchange processes (greenhouse gas emissions).
ISO 28902-2:2017 addresses manufacturers of heterodyne pulsed Doppler wind lidars, as well as bodies testing and certifying their conformity. Also, this document provides recommendations for the users to make adequate use of these instruments.
|
Published |
2017-07 |
Edition : 1 |
Number of pages : 39 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO 28902-3:2018 |
Air quality — Environmental meteorology — Part 3: Ground-based remote sensing of wind by continuous-wave Doppler lidar |
This document specifies the requirements and performance test procedures for monostatic heterodyne continuous-wave (CW) Doppler lidar techniques and presents their advantages and limitations. The term "Doppler lidar" used in this document applies solely to monostatic heterodyne CW lidar systems retrieving wind measurements from the scattering of laser light by aerosols in the atmosphere. Performances and limits are described based on standard atmospheric conditions. This document describes the determination of the line-of-sight wind velocity (radial wind velocity).
NOTE Derivation of wind vector from individual line-of-sight measurements is not described in this document since it is highly specific to a particular wind lidar configuration. One example of the retrieval of the wind vector can be found in ISO 28902-2:2017, Annex B.
This document does not address the retrieval of the wind vector.
This document can be used for the following application areas:
— meteorological briefing for e.g. aviation, airport safety, marine applications, oil platforms;
— wind power production, e.g. site assessment, power curve determination;
— routine measurements of wind profiles at meteorological stations;
— air pollution dispersion monitoring;
— industrial risk management (direct data monitoring or by assimilation into micro-scale flow models);
— exchange processes (greenhouse gas emissions).
This document can be used by manufacturers of monostatic CW Doppler wind lidars as well as bodies testing and certifying their conformity. This document also provides recommendations for users to make adequate use of these instruments.
|
Published |
2018-11 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.060
Geology. Meteorology. Hydrology
|
| ISO/TR 3985:2021 |
Biotechnology — Data publication — Preliminary considerations and concepts |
This document reviews best practices that:
a) respect the existing standardization efforts of life sciences research communities;
b) normalize key aspects of data description particularly at the level of the biology being studied (and shared) across the life sciences communities;
c) ensure that data are “findable” and useable by other researchers; and
d) provide guidance and metrics for assessing the applicability of a particular data sharing plan.
This document is applicable to domains in life sciences including biotechnology, genomics (including massively parallel nucleotide sequencing, metagenomics, epigenomics and functional genomics), transcriptomics, translatomics, proteomics, metabolomics, lipidomics, glycomics, enzymology, immunochemistry, life science imaging, synthetic biology, systems biology, systems medicine and related fields.
|
Published |
2021-05 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 5058-1:2021 |
Biotechnology — Genome editing — Part 1: Vocabulary |
This document defines terms related to genome editing technology.
This document is applicable to general use of genome editing across species.
|
Published |
2021-11 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO 5058-1:2021/Amd 1:2022 |
Biotechnology — Genome editing — Part 1: Vocabulary — Amendment 1 |
|
Published |
2022-07 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/CD 8472-1 |
Biotechnology — Data interoperability for stem cell data — Part 1: Framework |
This document provides a framework for data interoperability of stem cell data systems.
This document specifies considerations and requirements of stem cell data for data interoperability, such as characteristics, applied technologies, ethical requirements, and data sharing, analysis, accessibility.
This document describes an interoperable framework for stem cell data, which can be used for existing systems or existing architectures.
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/DTS 9491-1 |
Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models |
This document defines challenges and requirements for predictive computational models constructed for research purposes in personalized medicine. It specifies recommendations and requirements for the setup, formatting, validation, simulation, storing and sharing of such models, as well as their application in clinical trials and other research areas. It summarizes specific challenges regarding data input, as well as verifying and validating of such models that can be considered as best practices for modelling in research and development in the field of personalized medicine.
This document also specifies recommendations and requirements for data used to construct or needed for validating models, including rules and requirements for formatting, description, annotation, interoperability, integration, accessing, as well as recording and documenting the provenance of such data.
This document does not provide specific rules or requirements for the use of computational models in the clinical routine, or for diagnostic or therapeutic purposes.
|
Under development |
|
Edition : 1 |
Number of pages : 31 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/CD 18209-1 |
Biotechnology — Biobanking of parasites — Part 1: Helminths |
This document provides requirements for the biobanking of helminths as parasitic resources including the collection, safeguarding, classification, proliferation, preservation, storage, and distribution of helminths.
This document sets requirements for the quality of helminths and their associated data, the data collection, and safety management when handling the helminths as a source of human disease infection.
This document is applicable to all organizations performing biobanking with helminths used for research and development.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 18457:2016 |
Biomimetics — Biomimetic materials, structures and components |
ISO 18457:2016 provides a framework of biomimetics for the development of materials, structures, surfaces, components, and manufacturing technologies.
ISO 18457:2016 specifies the principles of biological systems, and especially the performance of biological materials, structures, surfaces, components, and manufacturing technologies that provide the motivation and reasons for biomimetic approaches. It specifies the methodology based on analysis of biological systems, which lead to analogies, and abstractions. The transfer process from biology to technology is described based on examples of biomimetic materials, structures, surfaces, components, and manufacturing technologies. This International Standard describes measurement methods and parameters for the characterization of properties of biomimetic materials. This International Standard provides information on the relevance of biomimetic materials, structures, surfaces, components, and manufacturing technologies for industry.
ISO 18457:2016 also links to other subareas in biomimetics because fundamental developments in materials, structures, surfaces, components, and manufacturing technologies often form the basis for a wide variety of additional innovations. It provides guidance and support for all those who develop, design, process, or use biomimetic materials, structures, surfaces, components, and manufacturing technologies. This International Standard can also serve for those who want to learn about and investigate these topics.
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Published |
2016-09 |
Edition : 1 |
Number of pages : 37 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 18458:2015 |
Biomimetics — Terminology, concepts and methodology |
ISO 18458:2015 provides a framework for the terminology on biomimetics in scientific, industrial, and educational purposes.
ISO 18458:2015 is intended to provide a suitable framework for biomimetic applications. The field of biomimetics is classified and defined, numerous terms are described, and a description of the process of applying biomimetic methods from the development of new ideas to the biomimetic product is provided. The limits and potential of biomimetics as an innovation approach or as a sustainability strategy are also illustrated. In addition, ISO 18458:2015 provides an overview of the various areas of application and describes how biomimetic methods differ from classic forms of research and development. If a technical system is subjected to a development process according to ISO 18458:2015, then it is allowed to be referred to as a "biomimetic" system.
ISO 18458:2015 provides guidance and support for developers, designers, and users who want to learn about the biomimetic development process and integrate biomimetic methods into their work aiming at a common language for scientists and engineers working in the field of biomimetics. It can be applied wherever nature has produced a biological system sufficiently similar to the technical target system that can be used to develop a technical equivalent.
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Published |
2015-05 |
Edition : 1 |
Number of pages : 25 |
Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO 18459:2015 |
Biomimetics — Biomimetic structural optimization |
ISO 18459:2015 specifies the functions and scopes of biomimetic structural optimization methods. They consider linear structural problems under static and fatigue loads. The methods described in ISO 18459:2015 are illustrated by examples.
The purpose of ISO 18459:2015 is to familiarize users with biomimetic optimization methods as effective tools for increasing the lifespan, reducing the weight of components, and promoting the widespread use of these methods in support of sustainable development.
ISO 18459:2015 is intended primarily for designers, developers, engineers, and technicians, but also for all persons entrusted with the design and evaluation of load-bearing structures.
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Published |
2015-05 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20387:2018 |
Biotechnology — Biobanking — General requirements for biobanking |
This document specifies general requirements for the competence, impartiality and consistent operation of biobanks including quality control requirements to ensure biological material and data collections of appropriate quality.
This document is applicable to all organizations performing biobanking, including biobanking of biological material from multicellular organisms (e.g. human, animal, fungus and plant) and microorganisms for research and development.
Biobank users, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others can also use this document in confirming or recognizing the competence of biobanks.
This document does not apply to biological material intended for food/feed production, laboratories undertaking analysis for food/feed production, and/or therapeutic use.
NOTE 1 International, national or regional regulations or requirements can also apply to specific topics covered in this document.
NOTE 2 For entities handling human materials procured and used for diagnostic and treatment purposes ISO 15189 and other clinical standards are intended to apply first and foremost.
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Published |
2018-08 |
Edition : 1 |
Number of pages : 36 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 14101:2012 |
Surface characterization of gold nanoparticles for nanomaterial specific toxicity screening: FT-IR method |
ISO/TS 14101:2012 provides guidelines for the identification of the surface bound molecules using FT-IR of dehydrated gold nanoparticle (AuNPs) films both before and after nanomaterial (NM) cytotoxicity testing.
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Published |
2012-11 |
Edition : 1 |
Number of pages : 23 |
Technical Committee |
07.120
Nanotechnologies
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| ISO/TS 20388:2021 |
Biotechnology — Biobanking — Requirements for animal biological material |
This document specifies requirements for the collection, reception, preparation, preservation, transport, storage, distribution, destruction and disposal of biological materials obtained from animals, excluding humans. Such resources include solid tissues, fluid samples and associated cells, excretory products and associated data.
This document is applicable to biological material or associated data, or both, that can be used for research and development and to biomolecules derived from the biological material, e.g. nucleic acids, proteins and metabolites.
This document is applicable to all organizations performing biobanking for research and development.
This document does not apply to biological material intended for food or feed production, laboratories undertaking analysis for food or feed production, or therapeutic use, or multiple of them.
This document does not apply to the establishment of cell lines derived from animal biological material.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
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Published |
2021-12 |
Edition : 1 |
Number of pages : 26 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20391-1:2018 |
Biotechnology — Cell counting — Part 1: General guidance on cell counting methods |
ISO 20391-1:2018 defines terms related to cell counting for biotechnology. It describes counting of cells in suspension (generally cell concentration) and cells adhered to a substrate (generally area density of cells). It provides key considerations for general counting methods (including total and differential counting, and direct and indirect counting) as well as for method selection, measurement process, and data analysis and reporting.
ISO 20391-1:2018 is applicable to the counting of all cell types ? mammalian and non-mammalian (e.g. bacteria, yeast) cells.
ISO 20391-1:2018 is not intended for counting of cells while in a tissue section or a biomaterial matrix.
Several sector/application-specific international and national standards for cell counting currently exist. When applicable, the user can consult existing standards when operating within their scope (specific measurement techniques and/or applications).
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Published |
2018-01 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20391-2:2019 |
Biotechnology — Cell counting — Part 2: Experimental design and statistical analysis to quantify counting method performance |
This document provides a method for evaluating aspects of the quality of a cell counting measurement process for a specific cell preparation through a set of quality indicators derived from a dilution series experimental design and statistical analysis. The quality indicators are based on repeatability of the measurement and the degree to which the results conform to an ideal proportional response to dilution. This method is applicable to total, differential, direct and indirect cell counting measurement processes, provided that the measurement process meets the criteria of the experimental design (e.g. cells are suspended in a solution).
This method is most suitable during cell counting method development, optimization, validation, evaluation and/or verification of cell counting measurement processes.
This method is especially applicable in cases where an appropriate reference material to assess accuracy is not readily available. This method does not directly provide the accuracy of the cell count.
This method is primarily applicable to eukaryotic cells.
NOTE Several sector/application specific international and national standards for cell counting exist. Where applicable, consulting existing standards when operating within their scope can be helpful.
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Published |
2019-08 |
Edition : 1 |
Number of pages : 53 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20395:2019 |
Biotechnology — Requirements for evaluating the performance of quantification methods for nucleic acid target sequences — qPCR and dPCR |
This document provides generic requirements for evaluating the performance and ensuring the quality of methods used for the quantification of specific nucleic acid sequences (targets).
This document is applicable to the quantification of DNA (deoxyribonucleic acid) and RNA (ribonucleic acid) target sequences using either digital (dPCR) or quantitative real-time PCR (qPCR) amplification technologies. It applies to target sequences present in nucleic acid molecules including double-stranded DNA (dsDNA) such as genomic DNA (gDNA) and plasmid DNA, single stranded DNA (ssDNA), complementary DNA (cDNA), and single stranded RNA (ssRNA) including ribosomal RNA (rRNA), messenger RNA (mRNA), and long and short non-coding RNA [microRNAs (miRNAs) and short interfering RNAs (siRNAs)], as well as double-stranded RNA (dsRNA).
This document applies to nucleic acids derived from biological sources such as viruses, prokaryotic and eukaryotic cells, cell-free biological fluids (e.g. plasma or cell media) or in vitro sources [e.g. oligonucleotides, synthetic gene constructs and in vitro transcribed (IVT) RNA].
This document is not applicable to quantification of very short DNA oligonucleotides (<50 bases).
This document covers:
— analytical design including quantification strategies (nucleic acid copy number quantification using a calibration curve as in qPCR or through molecular counting as in dPCR, quantification relative to an independent sample and ratio measurements) and use of controls;
— quantification of total nucleic acid mass concentration and quality control of a nucleic acid sample including assessment of nucleic acid quality (purity and integrity);
— PCR assay design, optimization, in silico and in vitro specificity testing;
— data quality control and analysis including acceptance criteria, threshold setting and normalization;
— method validation (precision, linearity, limit of quantification, limit of detection, trueness and robustness) with specific requirements for qPCR and dPCR;
— approaches to establishing metrological traceability and estimating measurement uncertainty.
This document does not provide requirements or acceptance criteria for the sampling of biological materials or processing of biological samples (i.e. collection, preservation, transportation, storage, treatment and nucleic acid extraction). Nor does it provide requirements and acceptance criteria for specific applications (e.g. food or clinical applications where specific matrix issues can arise).
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Published |
2019-08 |
Edition : 1 |
Number of pages : 50 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20397-1:2022 |
Biotechnology — Massively parallel sequencing — Part 1: Nucleic acid and library preparation |
This document specifies the general requirements for and gives guidance on quality assessments of nucleic acid samples. It specifies general guidelines for library preparations and library quality assessments prior to sequencing and data generation.
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Published |
2022-03 |
Edition : 1 |
Number of pages : 15 |
Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO/TS 17200:2013 |
Nanotechnology — Nanoparticles in powder form — Characteristics and measurements |
ISO/TS 17200:2013 lists fundamental characteristics which are commonly determined for nanoparticles in powder form. ISO/TS 17200:2013 prescribes specific measurement methods for each of these characteristics.
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Withdrawn |
2013-06 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO 20397-2:2021 |
Biotechnology — Massively parallel sequencing — Part 2: Quality evaluation of sequencing data |
This document specifies general requirements and recommendations for quality assessments and control of massively parallel sequencing (MPS) data. It covers post raw data generation procedures, sequencing alignments, and variant calling.
This document also gives general guidelines for validation and documentation of MPS data.
This document does not apply to any processes related to de novo assembly.
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Published |
2021-02 |
Edition : 1 |
Number of pages : 21 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 20399-1:2018 |
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 1: General requirements |
This document specifies definitions and general requirements for ancillary materials (AMs) used in cell processing of cellular therapeutic products.
This document is applicable to cellular therapeutic products, including those gene therapy products whereby cells form part of the final product. It does not apply to products without cells.
This document does not cover the selection, assessment or control of starting materials and excipients.
NOTE International, regional or national regulations or requirements can also apply to specific topics covered in this document.
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Withdrawn |
2018-11 |
Edition : 1 |
Number of pages : 10 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 20399-2:2018 |
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 2: Best practice guidance for ancillary material suppliers |
This document provides guidance for ancillary material (AM) suppliers to maintain a high level of lot-to-lot consistency in the aspects of identity, purity, stability, biosafety, performance, as well as the accompanying documentation.
This document is applicable to cellular therapeutic products, including gene therapy products whereby cells form part of the final product. It does not apply to products without cells.
The AMs described in this document include those of biological origin [e.g. sera, media (including media additives), growth factors, and monoclonal antibodies] and chemical origin. This document does not address dimethyl sulfoxide (DMSO) for cryopreservation, beads, scaffolds, feeder cells, apparatus and instruments, or additives used post bioprocessing.
This document does not cover the selection, assessment or control of starting materials and excipients.
NOTE International, regional or national regulations or requirements can also apply to specific topics covered in this document.
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Withdrawn |
2018-11 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 20399-3:2018 |
Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users |
This document provides guidance for ancillary material (AM) users. It is applicable to cellular therapeutic products, including those gene therapy products whereby cells form part of the final product. It does not apply to products without cells.
This document focuses primarily on ancillary materials (AMs) of biological (human and animal) origin and their potential impurities and contaminants.
NOTE 1 The decision chart in Figure 1 illustrates the rationale underlying the scope of this document.
However, diverse biological sources, including plants, insects and marine organisms, can also be used in the development of a cellular therapeutic product. Therefore the fundamental principles of risk management also apply for these sources of AMs.
This document does not cover the selection, assessment or control of starting materials and excipients. However, it is anticipated that these are still covered by general risk management procedures.
This document is applicable for users at all stages of clinical development and supply; however maximum benefits can be gained by the implementation of the recommendations in the early stages of development.
NOTE 2 International, regional or national regulations or requirements can also apply to specific topics covered in this document.
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Withdrawn |
2018-11 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20399:2022 |
Biotechnology — Ancillary materials present during the production of cellular therapeutic products and gene therapy products |
This document specifies requirements and gives guidance to suppliers and users of ancillary materials (AMs) to improve the consistency and quality of AMs of biological (human and animal) and chemical origin used in the production of cellular therapeutic products and gene therapy products for human use.
This document is applicable to materials that are used for cell processing and that come into contact with the active substance and that do not intentionally form part of the final cell and gene therapy product.
EXAMPLE 1 Reagents, anticoagulants, cytokines, growth factors, enzymes, antibodies, serum (human or bovine), buffered solutions, culture media, dishes (coated with biological material), beads (coated with biological material), cryoprotectants (agents for cryopreservation), activation agents/reagents, non-mammalian cell (e.g. insect cell, bacterial cell), plasmid, viral vector.
This document does not apply to materials that are not used for cell processing, materials that do not come into contact with the active substance, or materials that intentionally form part of the final cell and gene therapy product.
EXAMPLE 2 Cells that are either starting materials, intermediates or final form of a cellular therapeutic product, feeder cells, additives used post bioprocessing, scaffolds, non-biological consumables (e.g. beads, dishes, tissue culture flasks, bags, tubing, pipettes, needles), other plasticware that come into contact with the cell or tissue, apparatus, instruments.
A decision flowchart is given in Annex A.
NOTE International, regional or national regulations or requirements can also apply to specific topics covered in this document.
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Published |
2022-12 |
Edition : 1 |
Number of pages : 32 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 21899:2020 |
Biotechnology — Biobanking — General requirements for the validation and verification of processing methods for biological material in biobanks |
This document specifies the validation and verification requirements applicable to a biobank to be able to demonstrate that it operates its processing of biological materials with validated and/or verified methods that are fit for purpose.
This document is intended for use in the implementation and validation of processing methods for biological materials.
This document covers method validation and verification for the production of all biological materials. This document does not apply to biological material intended for food/feed production, laboratories undertaking food/feed analysis, and/or therapeutic use.
Reference material production is not covered in this document. For the production requirements for reference materials, see ISO 17034.
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Published |
2020-06 |
Edition : 1 |
Number of pages : 21 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20404:2023 |
Biotechnology — Bioprocessing — General requirements for the design of packaging to contain cells for therapeutic use |
This document specifies general requirements and considerations for the design of packaging used to contain cells for therapeutic use.
This document is applicable to packaging intended to contain the final products of cells for therapeutic use, as well as their starting and intermediate materials.
This document does not apply to:
a) receptacles used for processing cells in manufacturing processes, e.g. cell culture flask or bag;
b) shipping containers containing packages for transportation;
c) services that utilize packages, e.g. storage services.
NOTE 1 Examples of packaging, packages and shipping containers are illustrated in Annex A.
NOTE 2 The design of packaging includes processes to ensure that the designed packaging is manufactured to a required specification through trial manufacturing, testing and implementation of quality management.
NOTE 3 International, national or regional regulations or requirements can also apply to specific topics covered in this document.
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Published |
2023-04 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20688-1:2020 |
Biotechnology — Nucleic acid synthesis — Part 1: Requirements for the production and quality control of synthesized oligonucleotides |
This document specifies minimum requirements for the production and quality control of synthesized oligonucleotides (nominally up to 250 bases).
This document also describes general quality attributes for synthesized oligonucleotides as well as common methods for evaluating quality attributes.
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Published |
2020-02 |
Edition : 1 |
Number of pages : 28 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/DIS 20688-2 |
Biotechnology — Nucleic acid synthesis — Part 2: General definitions and requirements for the production and quality control of synthesized gene fragments, genes, and genomes |
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Under development |
|
Edition : 1 |
Number of pages : 28 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 20691:2022 |
Biotechnology — Requirements for data formatting and description in the life sciences |
This document specifies requirements for the consistent formatting and documentation of data and corresponding metadata (i.e. data describing the data and its context) in the life sciences, including biotechnology, and biomedical, as well as non-human biological research and development. It provides guidance on rendering data in the life sciences findable, accessible, interoperable and reusable (F-A-I-R).
This document is applicable to manual or computational workflows that systematically capture, record or integrate data and corresponding metadata in the life sciences for other purposes.
This document provides formatting requirements for both primary experimental or procedural data obtained manually and machine derived data. This document also describes requirements for storing, sharing, accessing, interoperability and reuse of data and corresponding metadata in the life sciences.
This document specifies requirements for large quantities of data systematically obtained from automated high throughput workflows in the life sciences, as well as requirements for large-scale and small-scale data sets obtained by other life science technologies and manual data capture.
This document is applicable to many domains in biotechnology and the life sciences including, but not limited to: basic/applied research in all domains of the life sciences, and industrial, medical, agricultural, or environmental biotechnology (excluding for diagnostic or therapeutic purposes), as well as methodology-driven domains, such as genomics (including massive parallel sequencing, metagenomics, epigenomics and functional genomics), transcriptomics, translatomics, proteomics, metabolomics, lipidomics, glycomics, enzymology, immunochemistry, synthetic biology, systems biology, systems medicine and related fields.
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Published |
2022-11 |
Edition : 1 |
Number of pages : 54 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 21709:2020 |
Biotechnology — Biobanking — Process and quality requirements for establishment, maintenance and characterization of mammalian cell lines |
This document specifies process and quality requirements for the biobanking of mammalian (including human) cell lines. It describes requirements for the fundamental procedures of the biobank handling cell lines, such as establishment, reception, identification, propagation, preservation, storage, quality control, and distribution of cell lines.
This document can be used by organizations performing biobanking activities with mammalian cell lines used for research and development, biobank users, organizations and schemes using peer-assessment and accreditation bodies.
This document does not apply to biological material intended for therapeutic use.
NOTE International, national or regional regulations or requirements can also apply to specific topics covered in this document.
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Published |
2020-11 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 21709:2020/Amd 1:2021 |
Biotechnology — Biobanking — Process and quality requirements for establishment, maintenance and characterization of mammalian cell lines — Amendment 1 |
|
Published |
2021-09 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 21710:2020 |
Biotechnology — Specification on data management and publication in microbial resource centers |
This document specifies requirements for data management and publication in microbial resource centres (MRCs) to enable consistent formatting, and a quality control workflow to improve the overall quality of data. It also provides recommendations for MRCs to improve data sharing and integration of microbial material and associated data.
This document is intended to facilitate procedures such as accessioning, acquisition, authentication, preservation, storage, and distribution, and can be used by MRCs, regulatory authorities, organizations, and schemes using peer-assessment to confirm or recognize the competence of MRCs in data management and publication
NOTE International, national and/or regional regulations or requirements can also apply to specific topics covered in this document.
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Published |
2020-11 |
Edition : 1 |
Number of pages : 25 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/CD TS 4958 |
Nanotechnologies — Liposomes terminology |
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO 21973:2020 |
Biotechnology — General requirements for transportation of cells for therapeutic use |
This document specifies general requirements and reviews the points to consider for the transportation of cells for therapeutic use, including storage during transportation.
Transportation starts from the transfer of the packaged cells by the sender to the transportation service provider and ends when the package is delivered to the receiver at its destination.
This document does not apply to transportation of cells within one facility.
This document includes the development of a transportation plan including verification and validation, communication between the client and the transportation service provider, and associated documentation.
This document does not specify particular conditions for transportation such as specification for shipping container, ambient temperature control, etc.
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Published |
2020-06 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TR 22758:2020 |
Biotechnology — Biobanking — Implementation guide for ISO 20387 |
This document provides guidance to biobanks on how to implement the quality management, management, and technical requirements of ISO 20387. It expands on aspects of ISO 20387 and provides examples for illustration purposes. The aim of this document is to assist biobanks to address competency of personnel and appropriate quality of biological material and data collections. This document is equally applicable to newly established and existing biobanks.
This document is applicable to all organizations performing biobanking, including biobanking of biological material from multicellular organisms (e.g., human, animal, fungus and plant) and microorganisms for research and development.
This document does not apply to biological material intended for feed/food production, laboratories undertaking analysis for food/feed production and/or therapeutic use.
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Published |
2020-05 |
Edition : 1 |
Number of pages : 23 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 22859:2022 |
Biotechnology — Biobanking — Requirements for human mesenchymal stromal cells derived from umbilical cord tissue |
This document specifies requirements for the biobanking of human mesenchymal stromal cells derived from umbilical cord tissue (i.e. Wharton’s jelly), further referred to as hUC-MSCs, including the collection of umbilical cord tissue and associated data, isolation, culture characterization, quality control, cryopreservation, storage, thawing, disposal, distribution and transport.
This document is applicable to all organizations performing biobanking of hUC-MSCs used for research and development.
This document does not apply to hUC-MSCs for the purpose of in vivo application in humans, clinical applications or therapeutic use.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
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Published |
2022-07 |
Edition : 1 |
Number of pages : 35 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 23033:2021 |
Biotechnology — Analytical methods — General requirements and considerations for the testing and characterization of cellular therapeutic products |
This document provides general requirements for the testing of cellular therapeutic products intended for human use.
This document also provides considerations for the characterization of cellular therapeutic products, including approaches to select and design analytical methods that are fit for purpose.
Such considerations can be used to establish critical quality attributes for a cellular therapeutic product.
This document is applicable to cellular starting materials (including those for tissue engineered products) and intermediates of cellular therapeutic products.
This document is not applicable to tissues used in transplantation.
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Published |
2021-08 |
Edition : 1 |
Number of pages : 35 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 23040:2021 |
Marine environment impact assessment (MEIA) — Specification for marine sediments in seabed areas — Survey of interstitial biota |
This document provides requirements and recommendations for conducting marine surveys of interstitial biota in marine sediments. It includes the specification of technical methods for the investigation of marine sediments, foraminifera, ostracoda, radiolaria, diatoms, coccoliths, sedimentary sporopollen, benthic viruses, benthic microbes (including bacteria, archaea and fungi), benthic microalgae, benthic protozoa and metazoan meiobenthos.
This document is applicable to marine surveys in diverse benthic habitats at any seabed, such as benthic sediments of coastal zones, shallow seas, or deep-sea waters.
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Published |
2021-12 |
Edition : 1 |
Number of pages : 102 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
13.020.99
Other standards related to environmental protection
;
47.020.99
Other standards related to shipbuilding and marine structures
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| ISO/TS 23105:2021 |
Biotechnology — Biobanking — Requirements for the biobanking of plant biological material for research and development |
This document specifies requirements for the collection, preparation, preservation, transportation, storage, distribution and disposal of plant biological materials and associated data.
This document is applicable only to biological material that can be used for further processing of biomolecules, e.g. nucleic acids, proteins and metabolites.
This document is applicable to all organizations performing plant biobanking for research and development.
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Published |
2021-10 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/CD 4962 |
Nanotechnologies — In vitro nanoparticle acute phototoxicity assay |
This document specifies a procedure to evaluate phototoxicity of nanoparticles (NPs), suspended in an aqueous environment, by measuring the relative reduction in cellular viability under near ultraviolet (UVA) irradiation.
The measurement is intended to assess the potential for acute photo-toxicity of nanomaterials. It is not designed to predict other joint effects of nanomaterials and light, such as genotoxicity, photoallergy or photomutagenicity. The method is also applicable to NP aggregates and agglomerates.
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Under development |
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Edition : 1 |
|
Technical Committee |
07.120
Nanotechnologies
|
| ISO/TS 23494-1:2023 |
Biotechnology — Provenance information model for biological material and data — Part 1: Design concepts and general requirements |
This document specifies a general concept for a provenance information model for biological material and data and requirements for provenance data interoperability and serialization.
The provenance information model covers any information relevant to the quality and fitness for purpose of the biological material generated throughout the preanalytical phase of the materials life cycle from collection to analysis, data originating from analytical procedures applied to the biological material and results from further mathematical processing of the data.
This document is applicable to organizations, authorities and industries that are:
a) collecting, processing or distributing biological material for research;
b) generating, collecting, analysing or storing data on biological material.
This document does not apply to biological material and data used for other than research or in fields that are regulated by national, regional or international laws, such as medical diagnosis and therapy or food production.
NOTE International, national, or regional regulations or requirements can also apply to specific topics covered in this document.
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Published |
2023-04 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/DTS 23511 |
Biotechnology — General requirements and considerations for cell line authentication |
This document defines terms related to cell line authentication in the field of biotechnology. This document describes the general principles, detection strategies and analytical methods for cell line authentication. This document provides requirements and considerations for method selection, quality control parameters, data analysis and reporting.
This document is applicable to routine inspection of cell lines in culture and in storage in the field of basic research, translational studies and product manufacturing.
This document is also applicable to cell line origin validation in academic and industrial laboratories, cell banks and manufacturing sites. This document is intended for mammalian cells, including human cells.
This document is not intended for non-animal cells (e.g. microbial contamination, plant cells), nor for cells in complex matrix (e.g. tissues, organs, organoids, plants).
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Under development |
|
Edition : 1 |
Number of pages : 18 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TS 23565:2021 |
Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use |
This document specifies minimum requirements and general considerations for equipment, consisting of hardware, software and consumables, used in the manufacturing of cells for therapeutic use. This includes equipment for processing cells for therapeutic use starting from cell isolation/selection, expansion, washing and volume reduction, from cell finish through to cryopreservation for the storage of cells for therapeutic use.
This document gives guidance on the design, use and maintenance of equipment and equipment systems to both suppliers and users from aspects including the target parties, i.e. supplier or user, and phase of involved task, i.e. design, use or maintenance.
This document is applicable to any unit operation system that is used, alone or in combination, for the manufacturing of cells for therapeutic use, meeting user requirements. It is applicable to devices used for the purpose of monitoring equipment status.
It does not apply to:
processing equipment for cells for therapeutic use used at the point of care;
devices used for analytical purposes;
biosafety cabinets, general cell culture equipment (such as CO2 incubators, etc.), and software to control multiple equipment systems or multiple unit operations.
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Published |
2021-10 |
Edition : 1 |
Number of pages : 18 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/TR 23845:2020 |
Biomimetics — Ontology-Enhanced Thesaurus (OET) for biomimetics |
This document describes prototypes of the Ontology-Enhanced Thesaurus (OET) and the Keyword Explorer interface to OET. Although their design philosophy is described, this document focuses on their value and how they work.
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Published |
2020-04 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO/TR 23846:2022 |
Biomimetics — Image search engine |
This document describes prototypes of the image search engine (ISE). It focuses on the use and value of ISE, but also describes its design principles.
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Published |
2022-07 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO/TR 23847:2022 |
Biomimetics — Integrating problem- and function-oriented approaches applying the TRIZ method |
This document describes prototypes of a database for developing biomimetic products with innovative problem-solving methods (TRIZ). The database has a mechanism to obtain the idea of technical problem-solving using the problem- and function-oriented approaches. This document focuses on the use and value of the database, but also describes its design principles.
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Published |
2022-07 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 24088-1:2022 |
Biotechnology — Biobanking of microorganisms — Part 1: Bacteria and archaea |
This document specifies requirements for the biobanking of bacteria and archaea. It includes management of microbial material associated data as well as biosafety and biosecurity requirements.
This document is applicable to all organizations performing biobanking with bacteria and archaea used for research and development.
This document does not apply to processing methods for microbial materials intended for food/feed production, laboratories undertaking food/feed analysis or therapeutic use.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
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Published |
2022-07 |
Edition : 1 |
Number of pages : 18 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/FDIS 24190 |
Biotechnology — Analytical methods — Risk-based approach for method selection and validation for rapid microbial detection in bioprocesses |
This document provides definitions, guidelines, a framework and a risk-based approach for the design, selection and validation for methods for rapid microbial detection cellular therapeutic product manufacturing.
This document contains the generalized requirements and risks associated with cellular therapeutic product manufacturing, with flexibility to address differences in specific manufacturing processes of each unique cellular therapeutic product.
This document primarily addresses sterility testing in cellular therapeutic product manufacturing. This document can be applied to other cell derived therapeutic product manufacturing.
This document focuses on rapid microbial test methods (RMTMs) used in both in-process and final product testing.
Viral testing in cell-based therapy manufacturing is not included in this document.
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Under development |
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Edition : 1 |
Number of pages : 44 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/DTS 24420 |
Biotechnology — Massively parallel DNA sequencing — General requirements for data processing of shotgun metagenomic sequences |
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Under development |
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Edition : 1 |
Number of pages : 18 |
Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO/FDIS 24421 |
Biotechnology — Minimum requirements for optical signal measurements in photometric methods for biological samples |
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Under development |
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Edition : 1 |
Number of pages : 35 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/CD 24479 |
Biotechnology — Minimum requirements for cellular morphological analysis — Image capture, image processing, and morphometry |
This document provides general requirements for cell morphometry to quantify cell morphological features including cell shape, size and texture.
This document addresses aspects of cell image capture using optical microscopy and image processing for morphometry.
This document defines terms and definitions corresponding to morphometric parameters, and lists the examples and their formulae, that represent quantitative cellular morphological features for evaluation of cell morphology in cell analysis.
This document is applicable to processed mammalian cells.
This document does not apply to clinical pathological analysis.
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Under development |
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Edition : 1 |
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Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/CD 24480 |
Biotechnology — Validation of Database used for nucleotide sequence evaluation |
This document describes a practical procedure for nucleotide sequence database evaluation and validation. This document describes minimum requirements for the validation of a nucleotide sequence database. This document is applicable only for databases consisting of entries of nucleotide sequences.
NOTE This document is not applicable to the general evaluation of the entire database quality including the quality of each data entry.
EXAMPLE The use of the validated database is for confirming a representative sequence specificity including primers or probes for qualification and quantification of target nucleic acids by conventional polymerase chain reaction (PCR), quantitative polymerase chain reaction (qPCR), digital polymerase chain reaction (dPCR) and microarray technologies.
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Under development |
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Edition : 1 |
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Technical Committee |
07.080
Biology. Botany. Zoology
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| ISO 24603:2022 |
Biotechnology — Biobanking — Requirements for human and mouse pluripotent stem cells |
This document specifies requirements for the biobanking of human and mouse pluripotent stem cells (PSCs), including the collection of biological source material and associated data, establishment, expansion, characterization, quality control (QC), maintenance, preservation, storage, thawing, disposal, distribution and transport.
This document is applicable to all organizations performing biobanking with human and mouse PSCs used for research and development.
This document does not apply to cell lines used for in vivo application in humans, clinical applications or therapeutic use.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
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Published |
2022-08 |
Edition : 1 |
Number of pages : 28 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO 24651:2022 |
Biotechnology — Biobanking — Requirements for human mesenchymal stromal cells derived from bone marrow |
This document specifies requirements for the biobanking of human mesenchymal stromal cells derived from bone marrow (hBM-MSCs), including the collection of bone marrow and associated data, isolation, culture, characterization, quality control, cryopreservation, storage, thawing, disposal, distribution and transport.
This document is applicable to all organizations performing biobanking with hBM-MSCs used for research.
This document does not apply to hBM-MSCs for the purpose of in vivo application in humans, cell therapy, clinical applications, tissue engineering or therapeutic use.
NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.
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Published |
2022-08 |
Edition : 1 |
Number of pages : 27 |
Technical Committee |
07.080
Biology. Botany. Zoology
|
| ISO/DTS 4971 |
Nanotechnologies — Performance evaluation of nanosuspensions containing clay nanoplates for quorum quenching |
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Under development |
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Edition : 1 |
Number of pages : 13 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO 19007:2018 |
Nanotechnologies — In vitro MTS assay for measuring the cytotoxic effect of nanoparticles |
ISO 19007:2018 specifies a method for evaluating the effects of nano-objects and their aggregates and agglomerates (NOAA) on cellular viability using the MTS assay. The assay design includes performance requirements and control experiments to identify and manage variability in the assay results.
ISO 19007:2018 is applicable to the use of a 96-well plate.
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Published |
2018-04 |
Edition : 1 |
Number of pages : 32 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/ASTM 51940:2002 |
Guide for dosimetry for irradiation of insects for sterile release programs |
ISO/ASTM 51940 outlines dosimetric procedures to be followed for the radiation sterilization of live insects for use in pest management programmes. The primary use of irradiated, reproductively sterile insects is in the Sterile Insect Technique, where large numbers of sterile insects are released into the field to mate with and thus control pest populations of the same species. A secondary use of irradiated insects is as benign hosts for rearing insect parasitoids. If followed, the procedures outlined in this International Standard will help to ensure that insects processed with ionizing radiation from gamma, electron or X-ray sources receive absorbed doses within a predetermined range.
ISO/ASTM 51940 covers dosimetry in the irradiation of insects for these types of irradiators: self-contained dry-storage 137Cs or 60Co irradiators, larger-scale gamma irradiators and electron accelerators. The absorbed dose for insect sterilization is typically within the range of 20 Gy to 600 Gy.
This International Standard specifically refers, throughout the text, to reproductive sterilization of insects. It is equally applicable to radiation sterilization of invertebrates from other taxa (for example, Acarina, Gastropoda) and to irradiation of live insects or other invertebrates for other purposes (e.g., inducing mutations), presuming the absorbed dose is within the range specified above.
It also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the insects have been irradiated.
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Withdrawn |
2002-03 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
17.240
Radiation measurements
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| ISO/ASTM 51940:2004 |
Guide for dosimetry for sterile insects release programs |
ISO/ASTM 51940:2004 outlines dosimetric procedures to be followed for the radiation sterilization of live insects for use in pest management programs. The procedures outlined in ISO/ASTM 51940:2004 will help ensure that insects processed with ionizing radiation from gamma, electron, or X-ray sources receive absorbed doses within a predetermined range. Information on effective dose ranges for specific applications of insect sterilization, or on methodology for determining effective dose ranges, is not within the scope of ISO/ASTM 51940:2004.
ISO/ASTM 51940:2004 covers dosimetry in the irradiation of insects for these types of irradiators: self-contained dry-storage 137Cs or 60Co irradiators, large-scale gamma irradiators, and electron accelerators. The absorbed dose for insect sterilization is typically within the range of 20 Gy to 600 Gy.
ISO/ASTM 51940:2004 refers, throughout the text, specifically to reproductive sterilization of insects. It is equally applicable to radiation sterilization of invertebrates from other taxa (for example, Acarina, Gastropoda) and to irradiation of live insects or other invertebrates for other purposes (for example, inducing mutations), provided the absorbed dose is within the range specified.
ISO/ASTM 51940:2004 also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the insects have been irradiated.
ISO/ASTM 51940:2004 does not purport to address all of the safety concerns, if any, associated with its use.
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Withdrawn |
2004-08 |
Edition : 2 |
Number of pages : 12 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
17.240
Radiation measurements
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| ISO/ASTM 51940:2013 |
Guide for dosimetry for sterile insects release programs |
ISO/ASTM 51940:2013 outlines dosimetric procedures to be followed for the radiation-induced reproductive sterilization of live insects for use in pest management programs. The primary use of such insects is in the Sterile Insect Technique, where large numbers of reproductively sterile insects are released into the field to mate with and thus control pest populations of the same species. A secondary use of sterile insects is as benign hosts for rearing insect parasitoids. The procedures outlined in this guide will help ensure that insects processed with ionizing radiation from gamma, electron, or X-ray sources receive absorbed doses within a predetermined range. Information on effective dose ranges for specific applications of insect sterilization, or on methodology for determining effective dose ranges, is not within the scope of this guide.
NOTE 1 — Dosimetry is only one component of a total quality assurance program to ensure that irradiated insects are adequately sterilized and fully competitive or otherwise suitable for their intended purpose.
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Withdrawn |
2013-04 |
Edition : 3 |
Number of pages : 12 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
17.240
Radiation measurements
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| ISO/ASTM 51940:2022 |
Guidance for dosimetry for sterile insects release programs |
1.1 This document outlines dosimetric procedures to be followed for the radiation-induced reproductive sterilization of live insects for use in pest management programs. The primary use of such insects is in the Sterile Insect Technique, where large numbers of reproductively sterile insects are released into the field to mate with and thus control pest populations of the same species. A secondary use of sterile insects is as benign hosts for rearing insect parasitoids. A third use is for testing detection traps for fruit flies and moths, and testing mating disruption products for moths. The procedures outlined in this document will help ensure that insects processed with ionizing radiation from gamma, electron, or X-ray sources receive absorbed doses within a predetermined range. Information on effective dose ranges for specific applications of insect sterilization, or on methodology for determining effective dose ranges, is not within the scope of this document.
NOTE 1—Dosimetry is only one component of a total quality assurance program to ensure that irradiated insects are adequately sterilized and fully competitive or otherwise suitable for their intended purpose.
1.2 This document provides information on dosimetry for the irradiation of insects for these types of irradiators: selfcontained dry-storage 137Cs or 60Co irradiators, self-contained low-energy X-ray irradiators (maximum processing energies from 150 keV to 300 keV), large-scale gamma irradiators, and electron accelerators (electron and X-ray modes).
NOTE 2—Additional, detailed information on dosimetric procedures to be followed in installation qualification, operational qualification, performance qualification, and routine product processing can be found in ISO/ASTM Practices 51608 (X-ray [bremsstrahlung] facilities processing at energies over 300 keV), 51649 (electron beam facilities), 51702 (large-scale gamma facilities), and 52116 (self-contained dry-storage gamma facilities), and in Ref (1)2 (self-contained X-ray facilities).
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard except for the non-SI units of minute (min) hour (h) and day (d). These non-SI units are accepted for use within the SI system.
1.4 This document is one of a set of standards that provides recommendations for properly implementing and utilizing radiation processing. It is intended to be read in conjunction with ISO/ASTM Practice 52628.
1.5 The absorbed dose for insect sterilization is typically within the range of 20 Gy to 600 Gy.
1.6 This document refers, throughout the text, specifically to reproductive sterilization of insects. It is equally applicable to radiation sterilization of invertebrates from other taxa (for example, Acarina, Gastropoda) and to irradiation of live insects or other invertebrates for other purposes (for example, inducing mutations), provided the absorbed dose is within the range specified in 1.5.
1.7 This document also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the insects have been irradiated (see ISO/ASTM Guide 51539).
1.8 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.9 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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Published |
2022-08 |
Edition : 4 |
Number of pages : 12 |
Technical Committee |
07.080
Biology. Botany. Zoology
;
17.240
Radiation measurements
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| ISO 6579:1990 |
Microbiology — General guidance on methods for the detection of Salmonella |
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Withdrawn |
1990-05 |
Edition : 2 |
Number of pages : 15 |
Technical Committee |
07.100
Microbiology
|
| ISO 7218:1985 |
Microbiology — General guidance for microbiological examinations |
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Withdrawn |
1985-09 |
Edition : 1 |
Number of pages : 14 |
Technical Committee |
07.100
Microbiology
|
| ISO 7251:1984 |
Microbiology — General guidance for enumeration of presumptive Escherichia coli — Most probable number technique |
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Withdrawn |
1984-11 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
07.100
Microbiology
|
| ISO 7402:1985 |
Microbiology — General guidance for the enumeration of enterobacteriaceae without resuscitation — MPN technique and colony count technique |
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Withdrawn |
1985-10 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
07.100
Microbiology
|
| ISO 7932:1987 |
Microbiology — General guidance for enumeration of Bacillus cereus — Colony count technique at 30 degrees C |
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Withdrawn |
1987-10 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
07.100
Microbiology
|
| ISO 15559:1998 |
Practice for use of a radiochromic optical waveguide dosimetry system |
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Withdrawn |
1998-12 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
17.240
Radiation measurements
|
| ISO/TS 4988:2022 |
Nanotechnologies — Toxicity assessment and bioassimilation of manufactured nano-objects in suspension using the unicellular organism Tetrahymena sp. |
This document provides a reliable and repeatable method for simultaneous assessment of both exposure and toxicity of manufactured nano-objects (MNOs) using Tetrahymena sp. The ingested, internalized material (MNOs) indicates aquatic exposure.
This document is intended to be used by all the centers working with nano(eco)toxicity of MNOs and capable of culturing of Tetrahymena sp. The method uses Tetrahymena sp. to assess exposure and effects of MNOs. In addition, the test can be used by centers (laboratories) interested in investigating the biological interaction of MNOs with living cells.
This method is applicable to nano-objects such as nanoparticles, nanofibres of certain size (in a µm size range), nanoplates, as well as their aggregates and agglomerates.
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Published |
2022-05 |
Edition : 1 |
Number of pages : 14 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/TS 5094:2023 |
Nanotechnologies — Assessment of peroxidase-like activity of metal and metal oxide nanoparticles |
This document specifies a method for assessing the peroxidase-like activity of metal and metal oxide nanoparticles by spectrophotometry. This document can serve as a reference for the measurements of peroxidase-like activities in other types of nanoparticles.
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Published |
2023-02 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/DTS 5387 |
Nanotechnologies — Lung burden mass measurement of nanomaterials for inhalation toxicity studies |
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Under development |
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Edition : 1 |
|
Technical Committee |
07.120
Nanotechnologies
|
| ISO/CD TS 7833 |
Nanotechnologies — Extraction method of nanomaterials from organs by proteinase K digestion |
This document specifies an extraction method of nanomaterials deposited in organs using the proteinase K.
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Under development |
|
Edition : 1 |
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Technical Committee |
07.120
Nanotechnologies
|
| ISO/DTS 10689 |
Nanotechnologies — Superhydrophobic surfaces and coatings: Characteristics and performance assessment |
This technical specification (TS) specifies the performance assessment method/s for superhydrophobic
surfaces and coatings subjected to mechanical stress, solar radiation and weathering, liquids, and
thermal cycling, where applicable based on the agreement between interested parties. The
performance assessment is carried out based on comparative measurements of the advancing and
receding angles and calculating the contact angle hysteresis before and after the above-mentioned
working/environmental conditions. This document does not address safety and environmental related
issues of such coatings.
Note 1. This TS is applicable to any superhydrophobic surfaces and coatings on which measuring the
advancing and receding angles is possible.
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Under development |
|
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/TS 10797:2012 |
Nanotechnologies — Characterization of single-wall carbon nanotubes using transmission electron microscopy |
ISO/TS 10797:2012 establishes methods for characterizing the morphology of single-wall carbon nanotubes (SWCNTs) and identifying the elemental composition of other materials in SWCNT samples, using transmission electron microscopy and chemical analysis by energy dispersive X-ray spectrometry.
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Published |
2012-06 |
Edition : 1 |
Number of pages : 33 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/TS 10798:2011 |
Nanotechnologies — Charaterization of single-wall carbon nanotubes using scanning electron microscopy and energy dispersive X-ray spectrometry analysis |
ISO/TS 10798:2011 establishes methods to characterize the morphology, and to identify the elemental composition of catalysts and other inorganic impurities in raw and purified single-wall carbon nanotube (SWCNT) powders and films, using scanning electron microscopy and energy dispersive X-ray spectrometry analysis.
The methods described in ISO/TS 10798:2011 for SWCNTs can also be applied to the analysis of multiwall carbon nanotubes (MWCNTs).
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Published |
2011-07 |
Edition : 1 |
Number of pages : 26 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO 10801:2010 |
Nanotechnologies — Generation of metal nanoparticles for inhalation toxicity testing using the evaporation/condensation method |
ISO 10801:2010 gives requirements and recommendations for generating metal nanoparticles as aerosols suitable for inhalation toxicity testing by the evaporation/condensation method. Its application is limited to metals such as gold and silver which have been proven to generate nanoparticles suitable for inhalation toxicity testing using the technique specified.
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Published |
2010-12 |
Edition : 1 |
Number of pages : 22 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO 10808:2010 |
Nanotechnologies — Characterization of nanoparticles in inhalation exposure chambers for inhalation toxicity testing |
ISO 10808:2010 specifies requirements for, and gives guidance on, the characterization of airborne nanoparticles in inhalation exposure chambers for the purpose of inhalation toxicity studies in terms of particle mass, size distribution, number concentration and composition.
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Published |
2010-12 |
Edition : 1 |
Number of pages : 18 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/TS 13830:2013 |
Nanotechnologies — Guidance on voluntary labelling for consumer products containing manufactured nano-objects |
ISO/TS 13830:2013 provides guidance on the content of voluntary labels for consumer products containing manufactured nano-objects.
|
Published |
2013-12 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
07.120
Nanotechnologies
|