ICH Q_ documents as guidance for all FDA regulated industries (not just pharmaceuticals)
Product Risk Management
Correcting problem-prone areas
Who should Attend
Regulatory Affairs, Senior management, Production, Quality Assurance, R&D and Engineering and other personnel involved in a U.S. FDA-regulated environment.
Past Events
Major CGMP Issues for 2012 - 10 Jan 2012, Webinar (22220)
Major CGMP Issues for 2026
Important
Please, check "Major CGMP Issues for" official website for possible changes, before making any traveling arrangements
