EU GMP Annex 1 Draft with Single-Use Systems
WEBINAR
The European Commission published a draft revision of the European Good Manufacturing Practice (GMP), Annex 1, on Manufacturing of Sterile Medicinal Products which will include specific guidance on the use and risk control of single-use systems. Here, it is emphasized that the use of closed systems such as single-use systems can reduce the risk of cross-contamination.
During this webinar, we will focus on points to consider assuring sterility and integrity of a single-use assembly, and how collaboration between supplier and end-user can support the overall contamination control strategy of final filtration and filling operation.
In this webinar, you will learn:
- What are the EU GMP Annex 1 draft expectations on the use and control of single-use systems
- Which measures to take assuring the integrity of a single-use system
- How collaboration between supplier and end-user can support a risk-based contamination control strategy
Speakers
Simone Biel, Ph.D.
Merck
Senior Regulatory Expert
Simone specializes in Single-Use Technology and filtration within biopharmaceutical manufacturing. She provides regulatory guidance to diverse stakeholders and has helped many drug manufacturers successfully implement Single-Use Technology. Her main focus is to ensure product performance meets quality and regulatory standards. Simone is an active member of the Parenteral Drug Association (PDA) and BioPhorum. She holds a Ph.D. in Microbiology from the University of Frankfurt.
Somasundaram G (Som)
Merck
Senior Consultant
Som is a consultant with customers for regulatory compliance, closed processing, and other areas in biopharmaceutical applications. He is also a member of PDA and ISPE industry associations. Som has worked in different functions within Merck for the last 19 years, including heading technology management, tech service, BioReliance® filter validation lab, commercial role, and business development areas. He also worked for a year in QA/QC as well as obtained one year of academic experience in microbiology.
Pharma and biopharma manufacturing
- Downstream Processing
Duration:1h 12min
Language:English
Session 1:presented April 26, 2022