• fda-import-program-2019-seminar-training
  • raw-material-requirements-health-canada-usp-ep-in-a-cgmp-environment-issues-and-solutions-

Webinars

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The Impact of ICH E6 R2

  • Pam Dellea Giltner
  • Aug 13, 2019

Seminars

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FDA's GMP Expectations for Phase I and First-in-Man Clinical Trials

  • Peggy Berry
  • San Francisco, CA | August 15-16, 2019

Quality Control Laboratory Compliance - cGMPs and GLPs

  • Kelly Thomas
  • Philadelphia, PA | August 19-20, 2019

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

  • David Nettleton
  • Philadelphia, PA | September 26-27, 2019

21 CFR Part 11 Compliance for SaaS/Cloud Applications

  • David Nettleton
  • Philadelphia, PA | September 26-27, 2019

Designing and Sustaining New and Existing Product Stability Testing Program

  • Charity Ogunsanya
  • Philadelphia, PA | September 26-27, 2019

FDA's New Import Program for 2019 - Strict Precision

  • Casper Uldriks
  • Houston, TX | October 17-18, 2019
  • reduce-costs-for-compliance-with-data-integrity
  • quality-control-laboratory-compliance-cgmps-and-glps

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