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EU GMP Updates


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Who should attend?

Personnel involved in QA, Quality Operations, Quality Release, QC, Manufacturing, Supply Chain

Details

Live Webinar
Date: May 3, 2018
Time: 11:00 AM ET | 8:00 AM PT
Duration: 60mins with Q&A

This webinar will cover an overview of EU GMP updates, including updates on Annex 1 Manufacture of Sterile Medicinal Products and upcoming Annex 21, GMP for Importers for Medicinal Products. The webinar will include information on the role of the Qualified Person (QP) in the EU and the challenges facing the QP. Hot topics from recent EU inspections will also be presented.

Areas Covered During The Session

Overview of EU GMP Updates

  • Reference Chapters & Annexes included and the current status of updates

Role of the QP in EU

  • Includes updates to recent Annex 16
  • Role of the QP in the Supply Chain

EU Inspection Hot Topics

  • Hot topics will be presented from recent EU inspections

Prices

Single Registration Single Attendee: $195.00 + HST CAD per session Single attendee refers to single participant at a single computer/login. Group Registration Group of 5 or less per location: $400.00 + HST CAD per session Group of 6 to 10 attendees per location: $750.00 + HST CAD per session Group of 11 to 20 attendees per location: per location: $1250.00 + HST CAD per session

Contact

IPA
enquiry@ipacanada.com

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