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  • data-integrity-fda-and-eu-regulatory-expectations
  • raw-material-requirements-fda-health-canada-ich-usp-ep-in-a-cgmp-environment

Webinars

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Seminars

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REACH and RoHS Compliance: Gain a Deeper Understanding

  • Kelly Eisenhardt
  • Virtual Seminar | August 24-25, 2020

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

  • Barry A Friedman
  • Virtual Seminar | August 24-25, 2020

Designing and Sustaining New and Existing Product Stability Testing Program

  • Charity Ogunsanya
  • Virtual Seminar | August 27-28, 2020

Quality Control Laboratory Compliance - cGMPs and GLPs

  • Kelly Thomas
  • Virtual Seminar | August 27-28, 2020

Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)

  • David L Chesney
  • Virtual Seminar | September 17-18, 2020

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

  • David Nettleton
  • Virtual Seminar | September 23-24, 2020

21 CFR Part 11 Compliance for SaaS/Cloud Applications

  • David Nettleton
  • Virtual Seminar | September 23-24, 2020

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

  • Rita Hoffman
  • Virtual Seminar | September 24-25, 2020

Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines

  • Mark Powell
  • Virtual Seminar | October 8-9, 2020

FDA Recalls - Before You Start, and After You Finish

  • Casper Uldriks
  • Virtual Seminar | October 8-9, 2020

Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)

  • Mark Powell
  • Virtual Seminar | October 19-20, 2020
  • reduce-costs-for-compliance-with-data-integrity
  • quality-control-laboratory-compliance-cgmps-and-glps

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