GRC Seminars

Upcoming Seminars

• PV (Pharmacovigilance) Audit Strategy Planning – A Practical Approach to Design and Implementation: 2-Day In-Person Seminar
  
  July 22-23, 2019 - San Francisco, CA
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• Employment Laws Certificate Program: 2 Days in person Seminar
  
  July 29-30, 2019 - Greenville, SC
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• Effective Quality Oversight of Pharmaceutical Contract Manufacturing Organizations (CMOs): 2-Day In-Person Seminar
  
  August 1-2, 2019 - Tampa, FL
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• eCTD Submissions of IND and NDA/BLA to the US FDA, EU and Canada: 2-Day In-Person Seminar by Ex-FDA Official
  
  August 5-6, 2019 - Newark, NJ
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• Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar
  
  August 8-9, 2019 - San Diego, CA
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• FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials: 2-Day In-Person Seminar by Ex-FDA Official
  
  August 15-16, 2019 - San Francisco, CA
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• Internal Audit, Fraud Risk Assessment and Risk Management Annual Plan: 2-Day Workshop
  
  August 15-16, 2019 - San Francisco, CA
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• Quality Control Laboratory Compliance – cGMPs and GLPs: One and a Half-day In-person Seminar
  
  August 19-20, 2019 - Philadelphia, PA
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• GMP Compliance for Quality Control and Contract Laboratories: 2-Day In-Person Seminar by Ex-FDA Director
  
  August 19-20, 2019 - Philadelphia, PA
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• Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina): 2-day In-person Seminar
  
  August 29-30, 2019 - Philadelphia, PA
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