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.
This video from GE Analytical Instruments highlights some key elements that can improve your cleaning validation program and will help you re-think the approach when using swabs for TOC analysis.
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.