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Revision Operations
07/12/2021 - 09:25 by Silke.Burghardt

Current revision
06/14/2021 - 11:14 by Silke.Burghardt

05/31/2021 - 13:17 by Silke.Burghardt

02/14/2021 - 15:52 by EVP

02/14/2021 - 15:51 by EVP

02/14/2021 - 15:42 by EVP

01/14/2021 - 20:25 by EVP

12/10/2020 - 17:21 by EVP

12/10/2020 - 17:18 by EVP

12/09/2020 - 22:32 by EVP

11/10/2020 - 14:59 by EVP

11/10/2020 - 14:56 by EVP

10/26/2020 - 09:36 by EVP

09/22/2020 - 18:14 by EVP

09/22/2020 - 18:12 by EVP

08/26/2020 - 18:51 by EVP

08/26/2020 - 18:50 by EVP

08/26/2020 - 18:45 by EVP

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EU GMP certificate with manufacturer's permit according to §13 AMG (German Drug Law) for the release of non-sterile pharmaceuticals (Leipzig plant)

DIN EN ISO 9001 | DIN EN ISO 13485 for medical devices | IFS Broker (HIgher Level)