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

European regulation on clinical trials 
  • June 7th, 2016
  • October 13th, 2016
  • December 6th, 2016
Managing post-authorization non-interventional studies
  • May 31th, 2016
  • November 17th, 2016
Clinical Quality Management System: Assessing the current situation, preparing an action plan, setting up a system or improving it.
  • June 13th and 14th, 2016
Preparing for Clinical Trial inspections (Sponsor and sites)
  • May 24th, 2016
How to conduct Clinical Trial Audits (documentation, sites, service providers, system audits)
  • June 21th and 22th, 2016
Computerized Systems Validation (CSV) as applied to Clinical Research and Pharmacovigilance – Introduction to approach and audits
  • October 6th and 7th, 2016
Norm ISO 9001 : 2015 “Quality Management Systems – Requirements” as applied to Clinical Research
  •  December 8th and 9th, 2016

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