08. - 10.06.2009

Brussels: GMP and GCP Compliance for Investigational Products

  • On 8 June 2009, Dr. Hiltrud Horn will give a one day- training course on the “How to successfully plan and start a clinical trial”. Her presentation will focus on the essentials of clinical trials and will give you practical advice on how to prepare the Clinical trials application (CTA) and how to successfully pass GCP-inspections.
  • On 10 June 2009, Dr. Horn will present information about “Managing the IMPD to ensure full clarification and compliance”.

For more information please visit the following website:
http://www.vibevents.com/pharma/ipcompliance/

(Conference organized by VIBpharma)



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