NF EN ISO 8871-4 : 2006
Current
The latest, up-to-date edition.
ELASTOMERIC PARTS FOR PARENTERAL AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 4: BIOLOGICAL REQUIREMENTS AND TEST METHODS
12-01-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Biological requirements
Annex A (informative) Test for extractable bacterial endotoxins
Annex B (normative) Test for cytotoxicity
Annex C (normative) Test for intracutaneous toxicity
Annex D (normative) Test for systemic toxicity
Bibliography
Describes biological requirements for elastomeric parts for parenterals and for devices for pharmaceutical use. It also specifies the test methods, i.e. it offers the extraction procedures for elastomeric parts, and it makes reference to relevant biological test instructions in Pharmacopoeias and standards.
| DevelopmentNote |
Indice de classement: S93-102-4 PR NF EN ISO 8871-4 August 2005. (08/2005) Supersedes NF EN ISO 8871. (11/2006)
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| DocumentType |
Standard
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| PublisherName |
Association Francaise de Normalisation
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| Status |
Current
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| Standards | Relationship |
| EN ISO 8871-4:2006 | Identical |
| BS EN ISO 8871-4:2006 | Identical |
| UNI EN ISO 8871-4 : 2006 | Identical |
| DIN EN ISO 8871-4:2006-09 | Identical |
| UNE-EN ISO 8871-4:2007 | Identical |
| ISO 8871-4:2006 | Identical |
| NF ISO 8362-5 : 2008 | INJECTION CONTAINERS AND ACCESSORIES - PART 5: FREEZE DRYING CLOSURES FOR INJECTION VIALS |
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