Superseded
Draft standard
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DIN EN 13824:2002-12
Sterilization of medical devices - Validation and routine control of aseptic processes - Requirements and guidance; German version prEN 13824:2002
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Summary
The document specifies requirements for the design and operation of aseptic processing facilities and the validation and routine control of aseptic processes for the preparation of sterile liquid medical devices. It is not intended to apply to pharmaceutical products where the requirements of the relevant good manufacturing practices are applicable.
Technical characteristics
| Publisher | Deutsche Institut für Normung e.V. (DIN) |
| Publication Date | 12/01/2002 |
| Cancellation Date | 02/01/2005 |
| Page Count | 0 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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