A full training program in Quality and Industry Regulations (Paris region – sessions conducted in French)

European regulation on clinical trials 
  • June 11th, 2015
  • September 24th, 2015
  • December 3rd, 2015
Managing post-authorization non-interventional studies
  • April 16th, 2015*
  • October 13th, 2015
Clinical Quality Management System: Assessing the current situation, preparing an action plan, setting up a system or improving it.
  • June 18th and 19th, 2015
Preparing for Clinical Trial inspections (Sponsor and sites)
  • March 12th, 2015
How to conduct Clinical Trial Audits (documentation, sites, service providers, system audits)
  • June 1st and 2nd, 2015
Computerized Systems Validation (CSV) as applied to Clinical Research and Pharmacovigilance – Introduction to approach and audits
  • October 5th and 6th, 2015
Preparing for a Pharmacovigilance Inspection: Inspector methods and expectations in the framework of the European regulations.
  • November 16th, 2015

* Course on April 9th is postponed due to announced national strike-out.

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Sunnikan is a training body (registered under number 11 94 04876 94 – this registration does not constitute State agreement).