Annual Pharmaceutical GMP Training Program; Comprehensive Training on the Most Up to Date FDA & Global GMP Requirements and Best Practices 8-Part Live Training Program (Over 20 Hours of Training and Live Q&A) - Instructors: Peter Calcott Ph.D. & Kim Huynh-Ba Human Errors in GMP Manufacturing and Laboratory Processes; Identification, Correction and Prevention, Latest FDA Regulatory Requirements & Most Common GMP Issues Caused by Human Error Instructor: Peter Calcott Ph.D. Meeting the Latest Regulatory GMP Requirements During Clinical Manufacturing, Understanding Key Differences in Implementing GMPs in Clinical vs. Commercial Manufacturing Instructor: Peter Calcott Ph.D. GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry Including a Review of the New 2018 MHRA Data Integrity Definitions & Guidances and the FDA’s Most Recent Draft Guidance Instructor: Peter Calcott Ph.D. Process Validation General Principles & Practices – Integrating the FDA and EU Guidance; ICH Q8, ICH Q9, ICH Q10 and Quality Metrics Instructor: Jerry Lanese Ph.D. FDA GMP Inspections; Preparations, Successful Strategies and Logistics Instructor: Jerry Lanese Ph.D.