+1-888-771-6965
Log In / Register

Your Shopping Cart

Contains 0 items
Total: $0.00
View Shopping Cart
  • data-integrity-fda-and-eu-regulatory-expectations
  • raw-material-requirements-fda-health-canada-ich-usp-ep-in-a-cgmp-environment

Webinars

View More »

Seminars

View More »

Data Integrity: FDA/EU Requirements and Implementation

  • Mark Powell
  • Virtual Seminar | July 14-15, 2020

A Comprehensive View of FDA Regulations for Medical Devices

  • Stephanie Harrell
  • Virtual Seminar | July 16-17, 2020

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

  • Barry A Friedman
  • Virtual Seminar | July 16-17, 2020

Quality Control Laboratory Compliance - cGMPs and GLPs

  • Kelly Thomas
  • Virtual Seminar | July 16-17, 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

Biostatistics for the Non-Statistician

  • Elaine Eisenbeisz
  • San Francisco, CA | July 23-24, 2020

Design Control Essentials for Medical Devices

  • Susanne Manz
  • Virtual Seminar | July 23-24, 2020
  • reduce-costs-for-compliance-with-data-integrity
  • quality-control-laboratory-compliance-cgmps-and-glps

You Recently Viewed