ISO 13926-2:2017
Current
The latest, up-to-date edition.
Pen systems — Part 2: Plunger stoppers for pen-injectors for medical use
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
English
28-11-2017
ISO 13926-2:2017 specifies the material, performance requirements and labelling and gives recommendations for shape and dimensions of plunger stoppers for pen-injectors for medical use.
NOTE The potency, purity, stability and safety of a medicinal product during its manufacture and storage can strongly be affected by the nature and performance of the primary packaging.
Committee |
ISO/TC 76
|
DevelopmentNote |
Supersedes ISO/DIS 13926-2. (11/2017)
|
DocumentType |
Standard
|
Pages |
7
|
PublisherName |
International Organization for Standardization
|
Status |
Current
|
Supersedes |
Standards | Relationship |
DIN ISO 13926-2:2018-07 | Identical |
NEN ISO 13926-2 : 2017 | Identical |
BS ISO 13926-2 : 2011 | Identical |
BS ISO 13926-2:2017 | Identical |
IS/ISO 13926 : Part 2 : 2017 | Identical |
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 13926-3:2012 | Pen systems Part 3: Seals for pen-injectors for medical use |
ISO 13926-1:2004 | Pen systems Part 1: Glass cylinders for pen-injectors for medical use |
ISO 2230:2002 | Rubber products — Guidelines for storage |
ISO 3302-1:2014 | Rubber — Tolerances for products — Part 1: Dimensional tolerances |
ISO 11608-3:2012 | Needle-based injection systems for medical use Requirements and test methods Part 3: Finished containers |
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 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 |
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