The recently published revision to Eudralex Vol. 4 Annex 1, clarified current expectations for the manufacture of sterile medicinal products in light of improved process understanding and advances in processing technologies.
This webinar will summarize important elements of this revision and highlight how single-use filtration systems can contribute to a holistic contamination control strategy helping drug manufacturers meet regulatory expectations.
In this webinar, you will:
- Receive a summary of key updates to EU GMP Annex 1
- Learn how your filtration systems can help meet the requirements of Annex 1
- Learn how comprehensive supplier testing information accelerates the implementation of single-use systems
Webinar Information
Pharma and biopharma manufacturing
- Downstream Processing
Doba trvání:1h
Jazyk:English
Relace 1:předložené February 2, 2023
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