CSA Group Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count ISO 8871-3:2003

Description
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. ISO 8871-3:2003 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.
Description
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. ISO 8871-3:2003 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.

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Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count - ISO 8871-3:2003 - CSA Group
Toronto, Ontario, Canada
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count
ISO 8871-3:2003
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count ISO 8871-3:2003
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. ISO 8871-3:2003 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.

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.

ISO 8871-3:2003 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.

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Technical Specifications

  CSA Group
Product Category Standards and Technical Documents
Product Number ISO 8871-3:2003
Product Name Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count
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