A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries elucidates how to train the man power involved in development, manufacturing, auditing, and validation of bio pharmaceuticals on a pilot scale, leading to scale-up production.
The 30 minute webinar reviews a summary of quantitative and qualitative validation cleaning techniques for both FDA and non-FDA customers. It is followed by questions and answers submitted during the live telecast.
Validation of Cleaning Programs is now a mandatory requirement under most GFSI food safety standards. Luckily, Safefood 360° has compiled everything you need to know to keep your external auditors more than happy.
Validation is a broad concept in the pharmaceutical manufacturing industry. It includes process validation, analytical method validation, equipment validation, cleaning validation and system validation.