Established, fully validated methodology and SOPs are required prior to initiation of any training activities.
Sam M. George
Advertisement
Articles by Sam M. George
Reserve samples of test and control articles must be retained for at least one stability time point after the completion of the study.
Advertisement
Latest Updated Articles
Expediting the Technical Transfer of Biopharmaceutical ProductsPublished: September 2nd 2006 | Updated:
The Laboratory Control System: Fulfilling cGMP RequirementsPublished: September 2nd 2006 | Updated:
Advertisement
Advertisement
Trending on BioPharm International
1
New Cellevate Nanofiber Microcarriers Aim to Transform Vaccine Manufacturing Processes
2
In KPMG's CEO Outlook, AI, Regulatory Demands, and Supply Chain Risk Rank High
3
Overcoming Funding Challenges and Maintaining Optimism in CGTs (Part 1)
4
Rentschler’s Time Capsule and How it Symbolizes European Biotech Progress
5
