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Recorded Webinars
Gina Reo | View Anytime | 60 Minutes
Developing an Environmental Monitoring Program Satisfying FDA's Listeria Monocytogenes
Robert J. Russell | View Anytime | 90 Minutes
EU Medical Device Regulation (MDR) - Updated CE Marking Process & ISO 13485:2016 Expectations
Robert J. Russell | View Anytime | 90 Minutes
Latin America Regulatory Compliance: Current Challenges in Argentina, Brazil and Mexico
Robert J. Russell | View Anytime | 3 Hours
3-Hour Virtual Seminar on Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Robert J. Russell | View Anytime | 90 Minutes
Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
Steven Wachs | View Anytime | 60 Minutes
Using Statistics to Determine Sample Size
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