RO
SR EN 13824:2005
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
This 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 applicable to those pharmaceutical products where the requirements of the relevant good manufacturing practices are applicable. NOTE Many of the principles included in this document can be applied to certain aseptically processed sterile solid medical devices.
Status :
Withdrawn
Approval date : 12/23/2005
Publish date : 12/25/2005
Withdrawal date : 10/31/2011
Number of pages : 63
ICS : 11.080.01 Sterilization and desinfectation
Technical Committee : 377 - Medical devices
- Replaced by SR EN ISO 13408-2:2011
- Replaced by SR EN ISO 13408-4:2011
- Replaced by SR EN ISO 13408-3:2011
- Replaced by SR EN ISO 13408-1:2011
- Replaced by SR EN ISO 13408-6:2011
- Replaced by SR EN ISO 13408-5:2011