| Name |
Description |
Abstract |
Status |
Publication date |
Edition |
Number of pages |
Technical committee |
ICS |
| ISO 11418-3:2005 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms |
ISO 11418-3:2005 specifies the design, dimensions, material and requirements of screw-neck glass bottles (veral) for pharmaceutical preparations in solid and liquid dosage forms. Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
ISO 11418-3:2005 is applicable to screw-neck glass bottles (veral) used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.
|
Withdrawn |
2005-02 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:2016 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms |
ISO 11418-3:2016 specifies the design, dimensions, material and requirements of screw-neck glass bottles (veral) for pharmaceutical preparations in solid and liquid dosage forms. Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
It is applicable to screw-neck glass bottles (veral) used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.
|
Published |
2016-11 |
Edition : 3 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:2016/Amd 1:2017 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms — Amendment 1 |
|
Published |
2017-11 |
Edition : 3 |
Number of pages : 2 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-4:1996 |
Containers and accessories for pharmaceutical preparations — Part 4: Tablet bottles |
Specifies the design, dimensions, materials and requirements of tablet bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of tablets which are not intended for parenteral use.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-5:1997 |
Containers and accessories for pharmaceutical preparations — Part 5: Dropper assemblies |
|
Withdrawn |
1997-12 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-5:2015 |
Containers and accessories for pharmaceutical preparations — Part 5: Dropper assemblies |
ISO 11418-5:2015 specifies the design, dimensions, material, and requirements of dropper assemblies consisting of a screw cap, dropper bulbs, and pipettes for the application and dosage of liquid pharmaceutical preparations.
This part of ISO 11418 is applicable to dropper assemblies used in the medical field in order to deliver pharmaceutical preparations contained in screw neck bottles according to ISO 11418-1.
Dropper assemblies are applicable to primary packs used in direct contact with the drug.
NOTE The potency, purity, stability, and safety of a drug during its manufacture and storage can be strongly affected by the nature and performance of the primary pack.
|
Published |
2015-03 |
Edition : 2 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-7:1998 |
Containers and accessories for pharmaceutical preparations — Part 7: Screw-neck vials made of glass tubing for liquid dosage forms |
|
Withdrawn |
1998-09 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-7:2016 |
Containers and accessories for pharmaceutical preparations — Part 7: Screw-neck vials made of glass tubing for liquid dosage forms |
ISO 11418-7:2016 specifies the design, dimensions, material and requirements of screw-neck vials for pharmaceutical preparations. Screw-neck vials are applicable to primary packs used in direct contact with a drug.
It applies to colourless or amber glass vials made from borosilicate or soda-lime-silica glass, made from glass tubing and intended to be used in the packaging, storage or transportation of pharmaceutical products.
NOTE The potency, purity, stability and safety of a drug during its manufacture and storage can be strongly affected by the nature and performance of the primary pack.
|
Published |
2016-06 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 15010:1998 |
Disposable hanging devices for transfusion and infusion bottles — Requirements and test methods |
|
Published |
1998-06 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| scrape failed |
Self-adhesive hanging devices for infusion bottles and injection vials — Requirements and test methods |
ISO 15137:2005 specifies requirements and test methods for self-adhesive hanging devices (SAHD) used in combination with infusion containers, e.g. infusion glass bottles (see ISO 8536-1).
The purpose of ISO 15137:2005 is to establish a safe SAHD for prescribed infusion containers while administering their content so as to ensure a safe application for the patient and for the user.
|
Published |
2005-07 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| scrape failed |
Self-adhesive hanging devices for infusion bottles and injection vials — Requirements and test methods |
ISO 15137:2005 specifies requirements and test methods for self-adhesive hanging devices (SAHD) used in combination with infusion containers, e.g. infusion glass bottles (see ISO 8536-1).
The purpose of ISO 15137:2005 is to establish a safe SAHD for prescribed infusion containers while administering their content so as to ensure a safe application for the patient and for the user.
|
Published |
2005-07 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| scrape failed |
Self-adhesive hanging devices for infusion bottles and injection vials — Requirements and test methods |
ISO 15137:2005 specifies requirements and test methods for self-adhesive hanging devices (SAHD) used in combination with infusion containers, e.g. infusion glass bottles (see ISO 8536-1).
The purpose of ISO 15137:2005 is to establish a safe SAHD for prescribed infusion containers while administering their content so as to ensure a safe application for the patient and for the user.
|
Published |
2005-07 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| scrape failed |
Self-adhesive hanging devices for infusion bottles and injection vials — Requirements and test methods |
ISO 15137:2005 specifies requirements and test methods for self-adhesive hanging devices (SAHD) used in combination with infusion containers, e.g. infusion glass bottles (see ISO 8536-1).
The purpose of ISO 15137:2005 is to establish a safe SAHD for prescribed infusion containers while administering their content so as to ensure a safe application for the patient and for the user.
|
Published |
2005-07 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 15747:2010 |
Plastic containers for intravenous injections |
ISO 15747:2010 contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals.
ISO 15747:2010 is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
|
Withdrawn |
2010-04 |
Edition : 2 |
Number of pages : 14 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 15747:2018 |
Plastic containers for intravenous injections |
This document specifies requirements to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals.
This document is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
NOTE In some countries, national or regional pharmacopoeias or other government regulations are legally binding and these requirements take precedence over this document.
|
Published |
2018-09 |
Edition : 3 |
Number of pages : 16 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 15759:2002 |
Medical infusion equipment — Plastics caps with inserted elastomeric liner for containers manufactured by the Blow-Fill-Seal (BFS) process |
|
Withdrawn |
2002-04 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 15759:2005 |
Medical infusion equipment — Plastics caps with inserted elastomeric liner for containers manufactured by the blow-fill-seal (BFS) process |
ISO 15759:2005 specifies the dimensional and functional requirements for plastics caps with inserted elastomeric liners, attached to the infusion container [blow-fill-seal (BFS) container] by welding or by collar technique. These caps are intended for use in the packaging and handling of liquid drugs for parenteral delivery.
|
Published |
2005-04 |
Edition : 2 |
Number of pages : 17 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/TR 19727:2017 |
Medical devices — Pump tube spallation test — General procedure |
ISO/TR 19727:2017 provides a method of measuring, analysing and assessing the particle shedding from an infusion pump set during pumping.
|
Published |
2017-08 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 11418-1:1996 |
Containers and accessories for pharmaceutical preparations — Part 1: Drop-dispensing bottles |
Specifies the design, dimensions, materials and requirements of drop-dispensing bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 21649:2006 |
Needle-free injectors for medical use — Requirements and test methods |
ISO 21649:2006 applies to safety and performance and testing requirements for single-use and multiple-use needle-free injection systems intended for human use in clinics and other medical settings and for personal use by patients.
The dose chamber of the injection system is often disposable and intended to be replaced after either a single use or a limited number of uses. It is sometimes separable from the injection mechanism and often termed a "cartridge", "ampoule", "syringe", "capsule" or "disc". In contrast, the dose chamber also may be a permanent internal chamber designed to last through the claimed life of the device.
|
Withdrawn |
2006-06 |
Edition : 1 |
Number of pages : 32 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 21649:2023 |
Needle-free injection systems for medical use — Requirements and test methods |
This document applies to safety and performance and testing requirements for single-use and multiple-use Needle-Free Injection Systems (NFISs) intended for human use in clinics and other medical settings and for personal use by patients.
The dose chamber of the NFIS is often disposable and intended to be replaced after either a single use or a limited number of uses. It is sometimes separable from the injection mechanism and often termed a “cartridge”, “ampoule”, “syringe”, “capsule” or “disc”. In contrast, the dose chamber can also incorporate a permanent internal chamber designed to last through the claimed life of the device, and an additional member or members which eliminate the risk of cross-contamination.
Excluded from this document are drug delivery methods which:
— involve penetration of a part of the device itself into or through skin or mucous membranes (such as needles, tines, micro-needles, implantable slow-release drug devices);
— generate aerosols, droplets, powders or other formulations for inhalation, insufflation, intranasal or oral deposition (such as sprays, inhalers, misters);
— deposit liquids, powders, or other substances on the surface of skin or mucosal surfaces for passive diffusion or ingestion into the body (such as transdermal patches, liquid drops);
— apply sonic or electromagnetic energy (such as ultrasonic or iontophoretic devices);
— infusion systems for adding or metering medication into or through systems of artificial tubes, catheters, and/or needles which themselves enter the body.
|
Published |
2023-01 |
Edition : 2 |
Number of pages : 36 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 22413:2007 |
Transfer sets for pharmaceutical preparations — Requirements and test methods |
ISO 22413:2006 applies to sterilized single use transfer sets that are used for pharmaceutical preparations.
|
Withdrawn |
2007-03 |
Edition : 1 |
Number of pages : 13 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 22413:2010 |
Transfer sets for pharmaceutical preparations — Requirements and test methods |
ISO 22413:2010 applies to sterilized single use transfer sets that are used for pharmaceutical preparations.
|
Withdrawn |
2010-06 |
Edition : 2 |
Number of pages : 13 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 22413:2021 |
Transfer sets for pharmaceutical preparations — Requirements and test methods |
This document specifies requirements and test methods for sterilized single-use transfer sets that are used for pharmaceutical preparations.
|
Published |
2021-06 |
Edition : 3 |
Number of pages : 14 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/TS 23128:2019 |
Medical devices — Transfusion set and blood bag compatibility test method |
This document details suitable equipment, a test method, acceptance criteria and advisable limits to help to ensure that there is compatibility (by measuring the insertion force) between a transfusion set closure piercing device (referred to in this document by the abbreviation 'spike') and a blood bag outlet port.
The test procedure in its entirety is complex and beyond the scope of each of the relevant transfusion set and blood bag standards. This document was therefore developed to support the implementation of the existing standards for blood bags and transfusion sets.
The procedure described in this document can be used by manufacturers of blood bags to test the compatibility with transfusion set spikes available on the market or by manufacturers of the transfusion set spikes to test the compatibility with blood bags available on the market.
|
Published |
2019-12 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/PRF 24072 |
Aerosol bacterial retention test method for air-inlet filter on administration devices |
|
Under development |
2023-06 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 28620:2010 |
Medical devices — Non-electrically driven portable infusion devices |
ISO 28620:2010 specifies essential requirements and related test methods for non-electrically driven portable infusion devices. It applies to devices designed for continuous (fixed or adjustable) flow and/or for bolus application.
These devices can be used in health care and non-health care settings. They can be applied or administered by health care professionals or by the intended patient.
These devices can be pre-filled by the manufacturer or filled before use by a health care professional or the intended patient.
|
Withdrawn |
2010-02 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 3004-1:1979 |
Hermetically sealed metal containers for food and drinks — Part 1: Round open-top general purpose food cans |
|
Withdrawn |
1979-02 |
Edition : 2 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 3004-1:1979/Amd 1:1981 |
Hermetically sealed metal containers for food and drinks — Part 1: Round open-top general purpose food cans — Amendment 1 |
|
Withdrawn |
1981-04 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 28620:2020 |
Medical devices — Non-electrically driven portable infusion devices |
This document specifies essential requirements and related test methods for non-electrically driven portable infusion devices, thereafter called "device".
It is applicable to devices designed for continuous (fixed or adjustable) flow and/or for bolus neuraxial and intravascular or hypodermic applications.
NOTE Sites for the neuraxial application include the spine, intrathecal or subarachnoid space, ventricles of the brain and the epi-, extra- or peri-dural space. Neuraxial application anaesthetics can be administered regionally, affecting a large part of the body, such as a limb, and include plexus blocks, such as the branchial plexus blocks or single nerve blocks. Neuraxial application procedures include continuous infusion of wounds with local anaesthetic agents.
These devices can be used in health care and non-health care settings. They can be applied or administered by health care professionals or by the intended patient.
These devices can be pre-filled by the manufacturer or filled before use by a health care professional or the intended patient.
This document does not apply to
— electrically driven or electrically controlled infusion pumps that are covered by IEC 60601-2-24,
— devices for single patient use intended to deliver discrete volumes (bolus) of medicinal product that are covered by the ISO 11608 series,
— implantable devices,
— enteral devices,
— transdermal delivery devices, and
— devices where the energy for infusion is not provided by the device or through active intervention by the patient (e.g. devices only powered by gravity).
|
Published |
2020-01 |
Edition : 2 |
Number of pages : 12 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 80369-1:2010 |
Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements |
ISO 80369-1:2010 specifies general requirements for small-bore connectors, which convey liquids or gases in healthcare applications. These small-bore connectors are used in medical devices or accessories intended for use with a patient.
ISO 80369-1:2010 also specifies the healthcare fields in which these small-bore connectors are intended to be used.
These healthcare fields of use include, but are not limited to, applications for:
breathing systems and driving gases,
enteral and gastric,
urethral and urinary,
limb cuff inflation,
neuraxial devices, and
intravascular or hypodermic.
Small-bore connectors as specified in ISO 80369-1:2010 are non-interconnectable with:
the cones and sockets of ISO 5356-1:2004 and ISO 5356-2:2006;
the temperature sensor connector and mating ports specified in Annex DD of ISO 8185:2007; and
the nipples of EN 13544-2:2002.
ISO 80369-1:2010 provides the methodology to assess non-interconnectable characteristics of small-bore connectors based on their inherent design and dimensions in order to reduce the risk of misconnections between medical devices or between accessories for different applications and to reduce the risk of misconnections between medical devices with 6 % Luer connectors, and all other non-Luer (6 %) connectors that will be developed under future parts of this series of standards.
It does not specify requirements for the medical devices or accessories that use these small-bore connectors. Such requirements are given in particular International Standards for specific medical devices or accessories.
|
Withdrawn |
2010-12 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
11.040.10
Anaesthetic, respiratory and reanimation equipment
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO 80369-1:2018 |
Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements |
This document specifies general requirements for small-bore connectors, which convey liquids or gases in healthcare applications. These small-bore connectors are used in medical devices or accessories intended for use with a patient.
This document also specifies the healthcare fields in which these small-bore connectors are intended to be used.
These healthcare fields include, but are not limited to:
— breathing systems and driving gases;
— enteral;
— limb cuff inflation;
— neuraxial;
— intravascular or hypodermic.
This document provides the methodology to assess non-interconnectable characteristics of small-bore connectors based on their inherent design and dimensions in order to reduce the risk of misconnections between medical devices or between accessories for different applications as specified in this document as well as those that will be developed under future parts of the ISO 80369 series.
This document does not specify requirements for the medical devices or accessories that use these small-bore connectors. Such requirements are given in particular International Standards for specific medical devices or accessories.
NOTE 1 Clause 7 allows for additional designs of small-bore connectors for new applications for inclusion in the ISO 80369 series.
NOTE 2 Manufacturers are encouraged to incorporate the small-bore connectors specified in the ISO 80369 series into medical devices, medical systems or accessories, even if currently not required by the relevant particular medical device standards. It is expected that when the relevant particular medical device standards are revised, the risks associated with changing to the new small-bore connectors as specified in the ISO 80369 series of standards will be considered.
NOTE 3 The connectors specified in the ISO 80369 series are intended for use only in their specified application. Use of these connectors for other applications increases risk that a hazardous misconnection could occur.
NOTE 4 Manufacturers and responsible organizations are encouraged to report their experience with the small-bore connectors specified in the ISO 80369 series to the Secretariat of ISO/TC 210 so that this feedback can be considered during the revision of the relevant part of the ISO 80369 series.
|
Published |
2018-11 |
Edition : 2 |
Number of pages : 31 |
Technical Committee |
11.040.10
Anaesthetic, respiratory and reanimation equipment
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/CD 80369-1.2 |
Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements |
|
Under development |
|
Edition : 3 |
|
Technical Committee |
11.040.10
Anaesthetic, respiratory and reanimation equipment
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/FDIS 80369-2 |
Small-bore connectors for liquids and gases in healthcare applications — Part 2: Connectors for respiratory applications |
|
Under development |
|
Edition : 1 |
|
Technical Committee |
11.040.10
Anaesthetic, respiratory and reanimation equipment
;
11.040.20
Transfusion, infusion and injection equipment
|
| ISO/DIS 80369-20 |
Small-bore connectors for liquids and gases in healthcare applications — Part 20: Common test methods |
|
Under development |
|
Edition : 2 |
Number of pages : 31 |
Technical Committee |
11.040.10
Anaesthetic, respiratory and reanimation equipment
;
11.040.20
Transfusion, infusion and injection equipment
;
11.040.25
Syringes, needles and catheters
|
| IWA 37-3:2022 |
Safety, security and sustainability of cannabis facilities and operations — Part 3: Good production practices (GPP) |
This document specifies requirements and recommendations for organizations directly or indirectly involved in the cannabis supply chain, to enable them to:
— plan, implement, operate, maintain and update a good production practice programme for providing products that are safe, according to their intended use;
— demonstrate compliance with applicable statutory and regulatory requirements;
— evaluate and assess mutually agreed customer requirements and demonstrate conformity to them;
— effectively communicate with interested parties and demonstrate conformity to relevant interested parties;
— demonstrate conformity to stated policies in a cannabis quality programme (CQP) for product safety, product quality, product security and facility safety;
— support the evaluation of quality programmes by external organizations or to permit self-assessment or self-declaration of adherence to some or all of the guidance contained in this document.
All requirements in this document are generic and intended to be applicable to all organizations in the cannabis supply chain, regardless of size and/or complexity. Organizations that are directly or indirectly involved include (but are not limited to) growers/cultivators, harvesters, primary processors, producers of cannabis, manufacturers of cannabis derivatives, cannabis edibles and/or cannabis products, testing providers, retailers and organizations providing transportation, storage and distribution services, suppliers of equipment, packaging materials and other contact materials.
This document intended to enable any organization, including small and/or less developed organizations, to implement externally developed elements in its CQP.
NOTE 1 Organizations in the cannabis supply chain are diverse in nature and not all the requirements specified in this document apply to each establishment or process. Justifications for exclusions or the use of alternative measures can be documented by a risk assessment/hazard analysis or other appropriate means.
This document provides guidance related to the following categories of cannabis, cannabis derivatives and cannabis products:
— cannabis plant seeds;
— cannabis plants;
— fresh cannabis;
— dried cannabis;
— cannabis derivatives;
— cannabis topicals;
— inhalable cannabis.
NOTE 2 Annex B provides additional guidance on applying GPP to cannabis edibles with respect to requirements and recommendations in existing food safety standards.
Where buildings or premises combine cultivation and processing of cannabis plants, including ancillary activities, along with other operational activities, the requirements and recommendations in this document apply only to that portion of the facility.
NOTE 3 Where joint use activities are present in a common building, specific statutory and regulatory requirements can apply for each category.
This document does not address the following:
— requirements related to research and development activities for finished products;
— general fire prevention or building construction features that are normally a function of local building and fire codes where applicable;
— premises used exclusively for operational activities, such as office space, call centres and retail outlets, used for the distribution, marketing, or sale of cannabis;
NOTE 4 Shipping and receiving of products from the production facility for further distribution are not considered as a retail outlet.
— the safe consumption or use of the cannabis or cannabis products produced by organizations applying these good production practices;
— occupational health and safety requirements governing cannabis workers and personnel except as identified in A.8.4 and A.8.6;
— the protection of the environment;
— security of the supply chain monitoring system, including cybersecurity and notifications;
NOTE 5 Security and monitoring of the supply chain are dealt with specifically in IWA 37-2.
— outdoor cultivation of cannabis and industrial hemp;
— growing of cannabis intended for personal use;
— the use of cannabinoids as ingredients that are derived from plants other than cannabis, or derived from other organisms, or created synthetically
|
Published |
2022-10 |
Edition : 1 |
Number of pages : 66 |
Technical Committee |
11.120.99
Other standards related to pharmaceutics
;
65.020.20
Plant growing
;
71.040.10
Chemical laboratories. Laboratory equipment
|
| ISO 3004-1:1986 |
Light gauge metal containers — Capacities and related cross-sections — Part 1: Open-top cans for general food |
|
Withdrawn |
1986-10 |
Edition : 3 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 11418-1:2005 |
Containers and accessories for pharmaceutical preparations — Part 1: Drop-dispensing glass bottles |
ISO 11418-1:2005 specifies the design, dimensions, material and requirements of drop-dispensing glass bottles. Drop-dispensing glass bottles are applicable to primary packs used in direct contact with a drug.
ISO 11418-1:2005 is applicable to drop-dispensing glass bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Withdrawn |
2005-02 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-1:2016 |
Containers and accessories for pharmaceutical preparations — Part 1: Drop-dispensing glass bottles |
ISO 11418-1:2016 specifies the design, dimensions, material and requirements of drop-dispensing glass bottles. Drop-dispensing glass bottles are applicable to primary packs used in direct contact with a drug.
It is applicable to drop-dispensing glass bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Published |
2016-11 |
Edition : 3 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-2:1996 |
Containers and accessories for pharmaceutical preparations — Part 2: Screw-neck bottles for syrups |
Specifies the design, dimensions, materials and requirements of screw-neck bottles used for pharmaceutical preparations in liquid form (sirups). Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-2:2005 |
Containers and accessories for pharmaceutical preparations — Part 2: Screw-neck glass bottles for syrups |
ISO 11418-2:2005 specifies the design, dimensions, material and requirements of screw-neck glass bottles for pharmaceutical preparations in liquid form (syrups). Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
ISO 11418-2:2005 is applicable to screw-neck glass bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Withdrawn |
2005-02 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-2:2016 |
Containers and accessories for pharmaceutical preparations — Part 2: Screw-neck glass bottles for syrups |
ISO 11418-2:2016 specifies the design, dimensions, material and requirements of screw-neck glass bottles for pharmaceutical preparations in liquid form (syrups). Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
It is applicable to screw-neck glass bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations which are not intended for parenteral use.
|
Published |
2016-11 |
Edition : 3 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-2:2016/Amd 1:2017 |
Containers and accessories for pharmaceutical preparations — Part 2: Screw-neck glass bottles for syrups — Amendment 1 |
|
Published |
2017-11 |
Edition : 3 |
Number of pages : 1 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:1996 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck bottles (veral) for solid and liquid dosage forms |
Specifies the design, dimensions, materials and requirements of screw-neck bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of solid and liquid pharmaceutical preparations which are not intended for parenteral use.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:2005 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms |
ISO 11418-3:2005 specifies the design, dimensions, material and requirements of screw-neck glass bottles (veral) for pharmaceutical preparations in solid and liquid dosage forms. Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
ISO 11418-3:2005 is applicable to screw-neck glass bottles (veral) used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.
|
Withdrawn |
2005-02 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:2016 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms |
ISO 11418-3:2016 specifies the design, dimensions, material and requirements of screw-neck glass bottles (veral) for pharmaceutical preparations in solid and liquid dosage forms. Screw-neck glass bottles are applicable to primary packs used in direct contact with a drug.
It is applicable to screw-neck glass bottles (veral) used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.
|
Published |
2016-11 |
Edition : 3 |
Number of pages : 6 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-3:2016/Amd 1:2017 |
Containers and accessories for pharmaceutical preparations — Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms — Amendment 1 |
|
Published |
2017-11 |
Edition : 3 |
Number of pages : 2 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-4:1996 |
Containers and accessories for pharmaceutical preparations — Part 4: Tablet bottles |
Specifies the design, dimensions, materials and requirements of tablet bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of tablets which are not intended for parenteral use.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-4:2005 |
Containers and accessories for pharmaceutical preparations — Part 4: Tablet glass bottles |
ISO 11418-4:2005 specifies the design, dimensions, material and requirements of tablet glass bottles. Tablet glass bottles are applicable to primary packs used in direct contact with a drug.
ISO 11418-4:2005 is applicable to tablet glass bottles used in pharmacy. Together with the corresponding closure systems, they serve for packaging of pharmaceutical preparations in solid and liquid dosage forms which are not intended for parenteral use.
|
Published |
2005-02 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-5:1997 |
Containers and accessories for pharmaceutical preparations — Part 5: Dropper assemblies |
|
Withdrawn |
1997-12 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-5:2015 |
Containers and accessories for pharmaceutical preparations — Part 5: Dropper assemblies |
ISO 11418-5:2015 specifies the design, dimensions, material, and requirements of dropper assemblies consisting of a screw cap, dropper bulbs, and pipettes for the application and dosage of liquid pharmaceutical preparations.
This part of ISO 11418 is applicable to dropper assemblies used in the medical field in order to deliver pharmaceutical preparations contained in screw neck bottles according to ISO 11418-1.
Dropper assemblies are applicable to primary packs used in direct contact with the drug.
NOTE The potency, purity, stability, and safety of a drug during its manufacture and storage can be strongly affected by the nature and performance of the primary pack.
|
Published |
2015-03 |
Edition : 2 |
Number of pages : 9 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-7:1998 |
Containers and accessories for pharmaceutical preparations — Part 7: Screw-neck vials made of glass tubing for liquid dosage forms |
|
Withdrawn |
1998-09 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 11418-7:2016 |
Containers and accessories for pharmaceutical preparations — Part 7: Screw-neck vials made of glass tubing for liquid dosage forms |
ISO 11418-7:2016 specifies the design, dimensions, material and requirements of screw-neck vials for pharmaceutical preparations. Screw-neck vials are applicable to primary packs used in direct contact with a drug.
It applies to colourless or amber glass vials made from borosilicate or soda-lime-silica glass, made from glass tubing and intended to be used in the packaging, storage or transportation of pharmaceutical products.
NOTE The potency, purity, stability and safety of a drug during its manufacture and storage can be strongly affected by the nature and performance of the primary pack.
|
Published |
2016-06 |
Edition : 2 |
Number of pages : 4 |
Technical Committee |
11.040.20
Transfusion, infusion and injection equipment
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 21976:2018 |
Packaging — Tamper verification features for medicinal product packaging |
This document specifies requirements and provides guidance for the application, use and check of tamper verification features to the packaging of medicinal products.
|
Published |
2018-11 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
55.020
Packaging and distribution of goods in general
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 23416:2023 |
General specifications and testing methods for temperature-sensitive medicinal packages in good distribution practice principles |
This document describes the general specifications of temperature-sensitive medicinal packaging based on the principles of good distribution practice (GDP). It also specifies test methods to validate the package performance for temperature-sensitive medicinal products. This covers the procedures of temperature-recording and testing methods on the performance of insulated containers such as dimensions, weights, storage capacity and robustness in temperature-controlling.
This document does not guarantee the quality and safety of all medicinal products. Under special circumstances where the weight or the characteristics of the products and environment show specific conditions, agreements are followed. This document does not cover the active packaging system, but only covers the passive packaging system able to control the desired temperature without any power sources.
|
Published |
2023-01 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
55.020
Packaging and distribution of goods in general
;
11.120.99
Other standards related to pharmaceutics
|
| ISO 24166-1:2022 |
Snap-on bottles for metering pumps — Part 1: Tubular glass |
This document specifies the shape, dimensions, fill capacities and performance requirements of tubular glass vials for metering pumps. It also specifies the material for the manufacturing of such containers as well as the secondary packaging.
This document provides also requirements for packaging of the tubular glass vials and addresses nonsterile, ready to sterilize or sterile as three possible options.
This document is applicable to colourless or amber containers made of tubular glass and intended to be used for packaging, storage or transportation of products intended for medicinal use.
|
Published |
2022-08 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
11.120.99
Other standards related to pharmaceutics
|
| ISO 24166-2:2022 |
Snap-on bottles for metering pumps — Part 2: Moulded glass |
This document specifies the shape, dimensions, fill capacities and performance requirements of moulded glass bottles for metering pumps. It also specifies the material for the manufacturing of such containers as well as the secondary packaging.
This document also provides requirements for packaging of the moulded glass bottles and addresses nonsterile, ready to sterilize or sterile as three possible options.
This document is applicable to colourless or amber glass containers moulded from borosilicate or soda-lime-silica glass and intended to be used in the packaging, storage or transportation of products intended for medicinal use.
|
Published |
2022-08 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
11.120.99
Other standards related to pharmaceutics
|
| ISO 24166-3:2022 |
Snap-on bottles for metering pumps — Part 3: Plastic |
This document specifies the shape, dimensions, fill capacities and performance requirements of plastic bottles for metering pumps. It also specifies the material for the manufacturing of such containers as well as the secondary packaging.
The document provides requirements for packaging of the plastic bottles and addresses nonsterile, ready to sterilize or sterile as three possible options.
This document is applicable to colourless or coloured containers moulded from plastic and intended to be used in the packaging, storage or transportation of products intended for medicinal use.
|
Published |
2022-08 |
Edition : 1 |
Number of pages : 18 |
Technical Committee |
11.120.99
Other standards related to pharmaceutics
|
| ISO 90-1:1986 |
Light gauge metal containers — Definitions and determination methods for dimensions and capacities — Part 1: Open-top cans |
|
Withdrawn |
1986-11 |
Edition : 1 |
Number of pages : 14 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 90-1:1997 |
Light gauge metal containers — Definitions and determination of dimensions and capacities — Part 1: Open-top cans |
|
Published |
1997-07 |
Edition : 2 |
Number of pages : 17 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 90-2:1986 |
Light gauge metal containers — Definitions and determination methods for dimensions and capacities — Part 2: General use containers |
|
Withdrawn |
1986-12 |
Edition : 1 |
Number of pages : 15 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 90-2:1997 |
Light gauge metal containers — Definitions and determination of dimensions and capacities — Part 2: General use containers |
|
Published |
1997-07 |
Edition : 2 |
Number of pages : 19 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 90:1977 |
Hermetically sealed metal cans for food and drinks — Specifications |
|
Withdrawn |
1977-06 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 1361:1983 |
Light gauge metal containers — Open-top cans — Round cans — Internal diameters |
|
Withdrawn |
1983-11 |
Edition : 3 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 1361:1997 |
Light-gauge metal containers — Round open-top cans — Internal diameters |
|
Published |
1997-12 |
Edition : 4 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 2735:1973 |
Hermetically sealed metal food containers — Capacities and diameters of round open-top and vent hole cans for milk |
|
Withdrawn |
1973-05 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 5099:2022 |
Light gauge metal containers — Easy-open ends and peel-off ends — Classification and dimensions |
This document specifies classification and the key dimensions of easy-open ends and peel-off ends.
This document is applicable to the manufacture and sale of easy-open ends and peel-off ends for food and beverages made of metal plates such as tin, chromium coated steel plates or aluminium alloy plates with a thickness of no more than 0,49 mm.
|
Published |
2022-07 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 7423:1982 |
Hermetically sealed metal containers for food and drinks — Food cans for fish and other fishery products — Sections for non-round cans |
|
Withdrawn |
1982-01 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 7670:1982 |
Hermetically sealed metal containers for food and drinks — Food cans for fish and other fishery products — Capacities of round and non-round cans and associated diameters of round cans |
|
Withdrawn |
1982-02 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 8610:1984 |
Light gauge metal containers — Round vent-hole cans with soldered ends for milk and milk products — Capacities and related diameters |
Lays down capacities and related diameters for vent-hole cans in common usage for milk and milk products. All can measurements in this Technical Report are given in accordance with the requirements of ISO 90-1.
|
Withdrawn |
1984-11 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 10193:2000 |
General use light gauge metal containers — Nominal filling volumes of round cylindrical and tapered containers of up to 40 000 ml |
This International Standard specifies a range of nominal filling volumes in common use for round cylindrical and
tapered general use containers of up to 40 000 ml volumetric capacity, metal thickness not exceeding 0,49 mm
nominal.
|
Withdrawn |
2000-10 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 10193:1989 |
Round general use light gauge metal containers — Nominal filling volumes and nominal diameters |
|
Withdrawn |
1989-12 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 10194:1989 |
Non-round general use light gauge metal containers — Nominal filling volumes and nominal cross-sections |
Gives a current list of nominal filling volumes and related nominal diameters. Concerns full friction can (cylindrical and tapered), friction closure can (cylindrical and tapered), and flat top can (cylindrical and tapered)
|
Withdrawn |
1989-08 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 10653:1993 |
Light-gauge metal containers — Round open-top cans — Cans defined by their nominal gross lidded capacities |
Specifies the nominal gross lidded capacities and related nominal diameters of the cans. Gross lidded capacities and tolerances shall be determined in accordance with ISO 90-1.
|
Published |
1993-04 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 10654:1993 |
Light-gauge metal containers — Round open-top cans — Cans for liquid products with added gas, defined by their nominal filling volumes |
Specifies the nominal filling volumes and related nominal diameters of the cans. Diameters shall be determined in accordance with ISO 90-1.
|
Published |
1993-04 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 11761:1992 |
Light-gauge metal containers — Round open-top cans — Classification of can sizes by construction type |
Gives a list of nominal gross lidded capacities and nominal diameters for round open top cans. Annex A gives a reference list to can sizes formerly standardized in ISO 3004, but now these cans do not meet the required criteria to be standardized and incorporated in ISO 10653.
|
Published |
1992-05 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 11762:1992 |
Light-gauge metal containers — Round open-top cans for liquid products with added gas — Classification of can sizes by construction type |
Gives a list of nominal filling volumes for the following containers: straight-sided cans, single necked-in cans, multiple necked-in cans. Annex A gives a reference list to can sizes formerly standardized in ISO 3004-3, but now these cans do not meet the required criteria to be standardized and incorporated in ISO 10654.
|
Published |
1992-05 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TR 11776:1992 |
Light gauge metal containers — Non-round open-top cans — Cans defined by their nominal capacities |
Gives a list of nominal capacities up to 2000 ml. Applies to the following shapes: rectangular, oval, obround, trapezoidal. Annex A gives a classification of can sizes by shapes with related nominal sections. Annex B lists can sizes previously standardized in ISO 3004-2, 3004-4 and 3004-5 and now excluded as they do not meet the required criterion of this report.
|
Withdrawn |
1992-10 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO/TS 21985:2022 |
Light gauge metal containers — Non-refillable LPG cartridges — General requirements |
This document specifies minimum requirements for the construction, design, material, performance, test methods and marking at manufacture of non-refillable liquefied petroleum gas (LPG) cartridges.
This document is applicable to non-refillable LPG cartridges which:
a) predominantly comprise butane fuel gas (iso/normal);
b) have a total nominal capacity of up to 250 g net;
c) are intended to deliver gas in the vapour state when either positioned upright or in a horizontal orientation;
d) are used with certain types of gas appliances, e.g. portable gas cookers;
e) are classified as UN 2037, RECEPTACLES, SMALL, CONTAINING GAS (GAS CARTRIDGES) without a release device, non-refillable for the transport of dangerous goods.
|
Published |
2022-02 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
55.120
Cans. Tins. Tubes
|
| ISO 24021-1:2022 |
Light gauge metal containers — Vocabulary and classification — Part 1: Open-top cans and ends |
This document defines terms and establishes a classification (see Annex A) for open-top metal cans and metal ends.
This document is applicable to open-top metal cans and metal ends for food and beverages made of metal plates such as tin or chromium-coated steel plates or aluminium alloy plates with a thickness of no more than 0,49 mm.
|
Published |
2022-08 |
Edition : 1 |
Number of pages : 31 |
Technical Committee |
55.120
Cans. Tins. Tubes
;
01.040.55
Packaging and distribution of goods (Vocabularies)
|
| ISO/CD 24021-2 |
Light gauge metal containers — Vocabulary and classification — Part 2: General cans |
This document specifies terminology and classification of general cans.
This document applies to hard metal containers used in food and chemical fields, with a nominal material thickness up to or equal to 0.49mm, made of tinplate or chromeplate sheet steel, and aluminium alloy sheets.
|
Under development |
|
Edition : 1 |
|
Technical Committee |
55.120
Cans. Tins. Tubes
;
01.040.55
Packaging and distribution of goods (Vocabularies)
|
| ISO 90-3:1986 |
Light gauge metal containers — Definitions and determination methods for dimensions and capacities — Part 3: Aerosol cans |
|
Withdrawn |
1986-12 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
55.130
Aerosol containers
|
| ISO 90-3:1986/Amd 1:1994 |
Light gauge metal containers — Definitions and determination methods for dimensions and capacities — Part 3: Aerosol cans — Amendment 1: Dimensions of the top end of three-piece necked-in tinplate cans |
|
Withdrawn |
1994-09 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.130
Aerosol containers
|
| ISO 90-3:2000 |
Light gauge metal containers — Definitions and determination of dimensions and capacities — Part 3: Aerosol cans |
|
Published |
2000-08 |
Edition : 2 |
Number of pages : 13 |
Technical Committee |
55.130
Aerosol containers
|
| ISO 10154:1991 |
Light gauge metal containers — Three-piece necked-in tinplate aerosol cans — Dimensions of the top end |
Specifies dimensions of cans with nominal internal body diameters ranging from 45 mm up to 65 mm. Figure 1 illustrates the shape.
|
Withdrawn |
1991-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
55.130
Aerosol containers
|
| ISO 13106:2014 |
Plastics — Blow-moulded polypropylene containers for packaging of liquid foodstuffs |
ISO 13106:2014 provides the requirements for polypropylene resins intended for use in blow-moulded, round containers with capacities up to, and including two litres intended for the packaging of liquids for human consumption. ISO 13106:2014 also provides tolerances on mass, dimensions, methods of sampling, testing, and performance requirements.
|
Published |
2014-05 |
Edition : 1 |
Number of pages : 18 |
Technical Committee |
55.140
Barrels. Drums. Canisters
;
83.140.99
Other rubber and plastics products
|
| ISO 15750-1:2002 |
Packaging — Steel drums — Part 1: Removable head (open head) drums with a minimum total capacity of 208 l, 210 l and 216,5 l |
This part of ISO 15750 specifies the characteristics and dimensions of removable head (open head) drums, manufactured from steel sheet, having a total capacity of 208 l, 210 l and 216,5 l.
It also specifies a method for measuring the total and brimful capacity.
|
Published |
2002-04 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 15750-2:2002 |
Packaging — Steel drums — Part 2: Non-removable head (tight head) drums with a minimum total capacity of 212 l, 216,5 l and 230 l |
This part of ISO 15750 specifies the characteristics and dimensions of non-removable head (tight head) drums, manufactured from steel sheet, having a total capacity of 212 l, 216,5 l and 230 l.
It also specifies a method for measuring the total capacity and brimful capacity, and a draining test method.
|
Published |
2002-04 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 15750-3:2002 |
Packaging — Steel drums — Part 3: Inserted flange-type closure systems |
This part of ISO 15750 specifies the characteristics, dimensions and finish of the inserted flange-type closure systems used for steel drums.
|
Withdrawn |
2002-04 |
Edition : 1 |
Number of pages : 43 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 15750-3:2022 |
Packaging — Steel drums — Part 3: Inserted flange-type closure systems |
This document specifies the characteristics, dimensions and finish of the inserted flange-type closure systems used for steel drums.
|
Published |
2022-05 |
Edition : 2 |
Number of pages : 36 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 20848-1:2006 |
Packaging — Plastics drums — Part 1: Removable head (open head) drums with a nominal capacity of 113,6 l to 220 l |
ISO 20848-1:2006 specifies the characteristics and dimensions of removable head (open head) plastics drums with a nominal capacity of 113,6 l to 220 l.
|
Published |
2006-09 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 20848-2:2006 |
Packaging — Plastics drums — Part 2: Non-removable head (tight head) drums with a nominal capacity of 208,2 l and 220 l |
ISO 20848-2:2006 specifies the characteristics and dimensions of non-removable head (tight head) plastics drums with a nominal capacity of 208,2 l and 220 l.
|
Published |
2006-09 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 20848-3:2006 |
Packaging — Plastics drums — Part 3: Plug/bung closure systems for plastics drums with a nominal capacity of 113,6 l to 220 l |
ISO 20848-3:2006 specifies the characteristics and dimensions of plug/bung closure systems for internally threaded openings in plastics drums of nominal capacity 113,6 l to 220 l.
|
Withdrawn |
2006-09 |
Edition : 1 |
Number of pages : 23 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 20848-3:2018 |
Packaging — Plastics drums — Part 3: Plug bung closure systems for plastics drums with a nominal capacity of 113,6 l to 220 l |
This document specifies the characteristics and dimensions of plug/bung closure systems for internally threaded openings in plastics drums of nominal capacity 113,6 l to 220 l.
|
Published |
2018-11 |
Edition : 2 |
Number of pages : 22 |
Technical Committee |
55.140
Barrels. Drums. Canisters
|
| ISO 1820:1975 |
Continuous mechanical handling equipment for loose bulk materials — Storage equipment : Storage bins and bunkers, silos and hoppers, bin gates — Safety code |
|
Withdrawn |
1975-10 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
53.080
Storage equipment
|
| ISO 5029:1977 |
Continuous mechanical handling equipment for loose bulk materials — Storage equipment fed by a pneumatic handling system — Safety code |
|
Withdrawn |
1977-05 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
53.080
Storage equipment
|
| ISO 8456:1985 |
Storage equipment for loose bulk materials — Safety code |
Gives special safety rules for storage equipment for loose bulk materials, such as hoppers, silos, storage bins and bunkers, and bin gates. These safety rules apply regardless of the use for which the equipment is intended.
|
Published |
1985-12 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
53.080
Storage equipment
|
| IWA 32:2019 |
Screening of genetically modified organisms (GMOs) in cotton and textiles |
This document provides requirements and recommendations to laboratories that perform genetically modified organism (GMO) analyses in cottonseed, leaf, cotton fibre and cotton fibre-derived materials.
The following are within the scope of this document:
a) identifying the materials to be assessed, based on the probability of obtaining good quality, fit for purpose DNA from the materials in subsequent steps in the cotton cloth production process;
b) specifying a method for efficient DNA isolation from cotton and cotton-derived materials described under point a);
c) specifying the cotton-specific method(s) to be used as control for amplifiable DNA;
d) specifying the screening procedure that provides optimal chances to detect GMOs as a result of the performance of the lowest number of genetically modified (GM) element screening assays.
NOTE 1 The protocol allows for the screening of all currently known GM cotton events and is set up in a way that optimizes the probability of also detecting unknown GM cotton events that possibly contain similar DNA sequences. Further information is given in CEN/TS 16707.
Sampling is outside of the scope of this document.
NOTE 2 A recommended sampling method is given in ISO 6497. General guidance for the sampling of bulk materials or for cotton-based products is available in standards such as ASTM D1441‑12 and CEN/TS 15568.
|
Published |
2019-04 |
Edition : 1 |
Number of pages : 31 |
Technical Committee |
59.020
Processes of the textile industry
|
| ISO 4921:1993 |
Knitting — Basic concepts — Vocabulary |
|
Withdrawn |
1993-10 |
Edition : 1 |
Number of pages : 27 |
Technical Committee |
59.020
Processes of the textile industry
;
01.040.59
Textile and leather technology (Vocabularies)
|
| ISO 4921:2000 |
Knitting — Basic concepts — Vocabulary |
This International Standard defines terms for basic knitting concepts.
The definitions of this vocabulary are complete in themselves; illustrations are used to clarify the content of a definition, but no standardization of any notational system is attempted.
|
Published |
2000-12 |
Edition : 2 |
Number of pages : 35 |
Technical Committee |
59.020
Processes of the textile industry
;
01.040.59
Textile and leather technology (Vocabularies)
|