GRC Seminars

Upcoming Seminars

• Fundamentals of EU MDR and IVDR – Level 1: 2-Day In-Person Seminar
  
  January 30-31, 2020 - Minneapolis, MN
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• Lifecycle Management of Analytical Methods and Procedures – according to new FDA and USP guidelines: 2-Day In-Person Seminar
  
  February 3-4, 2020 - San Francisco, CA
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• Managing Your Complaints and Obstacles in Post-Market Requirements — Results from Top Medical Device Observations During an Inspection: 2-day In-Person Seminar by Ex-FDA Official
  
  February 6-7, 2020 - Tampa, FL
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• Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar
  
  February 6-7, 2020 - San Francisco, CA
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• Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar
  
  February 6-7, 2020 - San Diego, CA
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• REACH and RoHS Compliance: Gain a Deeper Understanding: 2-Day In-Person Seminar
  
  February 6-7, 2020 - San Diego, CA
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• Analytical Instrument Qualification and System Validation: 2-Day In-Person Seminar
  
  February 6-7, 2020 - San Francisco, CA
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• FDA’s Medical Device Software Regulation Strategy: 2-Day In-Person Seminar by Ex-FDA Official
  
  February 13-14, 2020 - San Diego, CA
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• Designing and Sustaining New and Existing Product Stability Testing Program: 2-day In-person Seminar
  
  February 13-14, 2020 - San Francisco, CA
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• Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar
  
  February 20-21, 2020 - Salt Lake City, UT
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