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
Incoming search terms:
- société de conseil en affaires réglementaires pharma
- conseil affaires réglemenatires bpc