GRC Seminars

Upcoming Seminars

• FDA Audit, Quality Assurance Practices, Responsibilities and Expectations: 2 days in-person Seminar
  
  September 23-24, 2019 - San Francisco, CA
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• Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH): 2-Day Workshop
  
  September 23-24, 2019 - Singapore
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• Data Integrity: FDA/EU Requirements and Implementation: 2-Day Workshop
  
  September 25-26, 2019 - Singapore
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• The Veterinary Drug Approval Process and FDA Regulatory Oversight: 2-day In-Person Seminar
  
  September 26-27, 2019 - Kansas City, MO
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• Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR: 2-day In-person Seminar
  
  September 26-27, 2019 - Philadelphia, PA
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• 21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar
  
  September 26-27, 2019 - Philadelphia, PA
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• Designing and Sustaining New and Existing Product Stability Testing Program: 2-day In-person Seminar
  
  September 26-27, 2019 - Philadelphia, PA
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• Risk Management in Medical Devices Industry: 2-Day In-Person Seminar
  
  September 26-27, 2019 - Tampa, FL
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• Facility, Maintenance and Calibration Considerations of the Quality Systems Inspection Technique (QSIT): 2-Day In-Person Seminar
  
  October 2-3, 2019 - Philadelphia, PA
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• Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment – Issues and Solutions: 2-day In-person Seminar
  
  October 3-4, 2019 - San Diego, CA
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