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:

  • Submission to the Ethics Committee.
  • Submission to the National Order of Physicians Board
  • Submission to health authorities, such as the MSNA
  • Submission to the CNIL-France