Annex 1 Compliance: How Single-Use Technologies Are Simplifying Contamination Control
In this insightful webinar, delve into the evolving landscape of single-use technologies and their critical role in modern pharmaceutical manufacturing. With a particular focus on aseptic processing and the production of sterile drug substances and products, explore how these technologies align with the latest revisions to Annex 1 of the EU GMP guidelines. Gain a deeper understanding of regulatory expectations, risk mitigation strategies, and practical implementation approaches that ensure compliance while enhancing operational efficiency.
Whether you're involved in quality assurance, manufacturing, or regulatory affairs, learn how you can stay ahead in a rapidly changing industry.
Get unlimited access to:
Enter your credentials below to log in. Not yet a member of Bioprocess Online? Subscribe today.