CEN - EN ISO 8871-3
Elastomeric parts for parenterals and for devices for pharmaceuticals use - Part 3: Determination of released-particle count
active, Most Current
| Organization: | CEN |
| Publication Date: | 1 May 2004 |
| Status: | active |
| Page Count: | 14 |
| 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
EN ISO 8871-3
May 1, 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...
May 1, 2004
Elastomeric parts for parenterals and for devices for pharmaceuticals use - Part 3: Determination of released-particle count
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