ISO 8871-3
Elastomeric parts for parenterals and for devices for pharmaceutical use Part 3: Determination of released-particle count
active, Most Current
Buy Now
| Organization: | ISO |
| Publication Date: | 1 August 2003 |
| 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
January 1, 2018
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count AMENDMENT 1
A description is not available for this item.
ISO 8871-3
August 1, 2003
Elastomeric parts for parenterals and for devices for pharmaceutical 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...
August 1, 1990
Elastomeric Parts for Aqueous Parenteral Preparations
A description is not available for this item.