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  • 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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Seminars

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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

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

  • Barry A Friedman
  • San Diego, CA | October 3-4, 2019

Preparing for FDA's New Import/Export Trauma in 2020

  • Casper Uldriks
  • Dallas, TX | October 17-18, 2019

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

  • Penelope Przekop
  • Boston, MA | October 21-22, 2019

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

  • Peggy Berry
  • San Francisco, CA | November 7-8, 2019

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

  • Rita Hoffman
  • Boston, MA | November 14-15, 2019

Quality Control Laboratory Compliance - cGMPs and GLPs

  • David L Chesney
  • San Francisco, CA | November 18-19, 2019
  • reduce-costs-for-compliance-with-data-integrity
  • quality-control-laboratory-compliance-cgmps-and-glps

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