cGMP Regulatory 2020 - What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections Live Webinar

Join us for a webinar on September 15 for a discussion of the webinar
GMP-compliance is a must for manufacturers of finished pharmaceutical products and active pharmaceutical ingredients (APIs) according to the different national legislations.
It has often been stated that “FDA inspects for compliance; European inspectors inspect for adequate science”.
U.S., EU and Japan GMPs - Status of Harmonization& Future Trends
Current status of harmonization of GMP requirements
Future Trends
Where Inconsistencies Become a Problem: WHO, ICH, Countries
Discrepancies in global expectations
Alignment issues
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations