Charles River Laboratories will be sponsoring the upcoming 2021 Asia Pacific PDA Pharmaceutical Manufacturing & Quality Virtual Conference. This three-day event will cover the evolving landscape of GMP regulations (especially Annex 1 requirements), key trends in barrier technology for sterile manufacturing as well as rapid microbiology in QC, which is of increasing interest in delivering speed for COVID-19 vaccine manufacturing, and cell and gene therapy.
Thought leaders in the industry will present on topics including:
- Regulatory and compendial updates
- Implementation of Annex 1 and PUPSIT in sterile manufacturing
- New technology in aseptic processing
- Contamination control strategy
- Environmental monitoring and rapid microbiological methods
As part of the agenda, we invite you to attend the following presentation on Thursday, September 16 as part of the Rapid Microbiology and Automation session:
Rapid Micro Method Application | Jonas Van Den Berg, Quality Manager, Global Quality Control
Whether you’re still in development or already manufacturing, our Microbial Solutions services provide state-of-the-art technology and expert regulatory advice that will help you anticipate challenges, avoid roadblocks, and make better decisions. If you have any questions, please reach out to us at [email protected].