ANSI/AAMI/ISO 13408-1:2008(R2017)/A1:2013
Superseded
View Superseded by
Aseptic processing of health care products -- Part 1: General requirements (includes Amendment 1).
English
05-18-2017
08-03-2024
This part of ISO 13408 specifies the general requirements for, and offers guidance on, processes, programs and procedures for development, validation and routine control of the manufacturing process for aseptically-processed health care products.
| Committee |
TC 198
|
| DocumentType |
Standard
|
| ISBN |
978-1-57020-326-8
|
| Pages |
79
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 13408-1:2008/Amd 1:2013 | Identical |
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