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QP release – expectations and responsibilities for clinical and commercial drug products in Europe

Event Start Date: 23/06/2021 10:00

Event End Date: 23/06/2021 11:00

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Overview: This webinar will address European GMP requirements and the role and responsibilities of the QP:

  • Expectations and responsibilities of the QP for release of drug product for clinical trials and commercial supply in EU
  • New regulatory horizons in the UK & how to ensure supply continuity across Europe
  • Best practices required to efficiently gain QP release – for clinical and commercial products manufactured in North America and other countries outside the EU
  • Case studies to demonstrate the seamless process of QP release and timely supply