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As this is not your first time here, you may want to read our white paper which explains how to have a successful clinical study. click here to download the white paper for free! 🙂

Your regulatory affairs under control


We want your regulatory affairs to be managed optimally. We ensure strict monitoring of your trials to full compliance with the requirements of clinical research sector.

For this, we prepare your files according to European directives and regulations in force:

bmission to the Ethics Committee.

  • Submission to the National Order of Physicians Board
  • Submission to Health authorities and Ethics Committee
  • Submission to the CNIL-France

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