GRC Seminars

Upcoming Seminars

• Managing Your Complaints and Obstacles in Post-Market Requirements — Results from Top Medical Device Observations During an Inspection: One and a Half-day In-Person Seminar by Ex-FDA Official
  
  October 18-19, 2018 - Minneapolis, MN
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• Designing and Sustaining New and Existing Product Stability Testing Program: 2-day In-person Seminar
  
  October 18-19, 2018 - Orlando, FL
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• PV (Pharmacovigilance) Audit Strategy Planning – A Practical Approach to Design and Implementation: 2-Day In-Person Seminar
  
  October 25-26, 2018 - San Francisco, CA
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• Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar
  
  November 1-2, 2018 - Boston, MA
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• Project Management in Clinical Research: 2-Day In-Person Seminar
  
  November 1-2, 2018 - San Francisco, CA
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• Computer System Validation – Reduce Costs and Avoid 483s: 2-day In-person Seminar
  
  November 6-7, 2018 - San Francisco, CA
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• 21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar
  
  November 6-7, 2018 - San Francisco, CA
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• Supplier Management for Medical Device Manufacturers: 2-day In-person Seminar
  
  November 8-9, 2018 - Boston, MA
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• Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment – Issues and Solutions: 2-day In-person Seminar
  
  November 8-9, 2018 - Orlando, FL
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• Complete 1099, TIN Matching, B-Notice, FATCA and Nonresident Alien 1042-S Compliance Update: 2-Day In-Person Seminar
  
  November 8-9, 2018 - Columbia, SC
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