Ø Writing and implementation of SOPs in Clinical research according to the Good Clinical Practices,

       ICH and your working methods.

                  o  Monitoring in clinical research (pre-study, implementation, follow-up and  close out

                      visits)

                  o    Informed Consent

                  o    Safety data

                  o    Regulatory submissions

 Ø Leading of training about SOPs and regulatory

 Ø Regular monitoring of changes of European and French regulations

   Services offered to conduct your studies in clinical research

  Ø Monitoring in clinical research 
  Ø Clinical trial coordination
  Ø Training in clinical research
  Ø Regulatory submission of clinical trial