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EN ISO 8362-2:2015

Withdrawn

Withdrawn

Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2015)

Published date

10-28-2015

Withdrawn date

04-30-2016

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European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Classification
4 Shape and dimensions
5 Designation
6 Material
7 Performance requirements
8 Labelling
Bibliography

ISO 8362-2:2015 specifies the shape, dimensions, material, performance requirements and labelling of closures for injection vials covered by ISO 8362‑1 and ISO 8362‑4.The dimensional requirements are not applicable to barrier-coated closures.Closures specified in ISO 8362-2:2015 are intended for single use only.

Committee
CEN/BT
DevelopmentNote
Supersedes EN 28362-2. (09/2010)
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Withdrawn
Supersedes

ISO 8871-1:2003 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 1: Extractables in aqueous autoclavates
ISO 7619-1:2010 Rubber, vulcanized or thermoplastic — Determination of indentation hardness — Part 1: Durometer method (Shore hardness)
ISO 2230:2002 Rubber products — Guidelines for storage
ISO 8362-4:2011 Injection containers and accessories — Part 4: Injection vials made of moulded glass
ISO 3302-1:2014 Rubber — Tolerances for products — Part 1: Dimensional tolerances
ISO 15378:2017 Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
ISO 8362-1:2009 Injection containers and accessories — Part 1: Injection vials made of glass tubing
ISO 3302-2:2008 Rubber — Tolerances for products — Part 2: Geometrical tolerances
ISO 8871-5:2016 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing
ISO 48:2010 Rubber, vulcanized or thermoplastic — Determination of hardness (hardness between 10 IRHD and 100 IRHD)
ISO 8871-4:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 4: Biological requirements and test methods

Sorry this product is not available in your region.