DS/EN ISO 8871-3
Elastomeric parts for parenterals and for devices for pharmaceutical use – Part 3: Determination of released-particle count – Amendment 1 (ISO 8871-3:2003/Amd 1:2018)
active, Most Current
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| Organization: | DS |
| Publication Date: | 1 April 2019 |
| Status: | active |
| Page Count: | 12 |
| ICS Code (Transfusion, infusion and injection equipment): | 11.040.20 |
scope:
Elastomeric closures may be superficially contaminated with visible and subvisible particles, and fragments can also be produced when the closure is pierced by a needle. Such particles may be transferred to pharmaceutical preparations in contact with the elastomeric parts and affect the quality of such preparations. This part of ISO 8871 specifies methods for the determination of the number of visible and subvisible particles, respectively, detached from elastomeric parts by rinsing. It does not specify particle contamination limits. These will have to be agreed upon between manufacturer and user.
Document History
DS/EN ISO 8871-3
April 1, 2019
Elastomeric parts for parenterals and for devices for pharmaceutical use – Part 3: Determination of released-particle count – Amendment 1 (ISO 8871-3:2003/Amd 1:2018)
Elastomeric closures may be superficially contaminated with visible and subvisible particles, and fragments can also be produced when the closure is pierced by a needle. Such particles may be...
November 22, 2004
Elastomeric parts for parenterals and for devices for pharmaceuticals use - Part 3: Determination of released-particle count
Elastomeric closures may be superficially contaminated with visible and subvisible particles, and fragments can also be produced when the closure is pierced by a needle. Such particles may be...