Welcome to CC, Our Activity

CC Clinical research Consultants is a clinical and regulatory affairs CRO (Contract Research Organization), based in central Paris, that provides clinical trials support to the Medical Industries

  • Need a CRO to take full charge of your trial in Europe or Worldwide ?
  • Need strong expertise in designing a trial and setting it up according to your needs and running it in an unknown regulatory environment ?
  • Need someone to take the burden off your shoulders for interfacing with busy medical experts ?
  • Need a specific task to be completed within a trial you are running internally or have already assigned to another CRO ?
  • Tired of dealing with an undefined team, innumerable individuals, constant turnover, remote management ?
  • Tired of constantly expanding budgets whereas the initial quote you had chosen was meant to be the cheapest ?
  • Puzzled by changing regulatory environments and innumerable submissions ?
  • Need a VP-Level Transitional Manager to take over for a defined period of time the direction of your Euopean or Local clinical team?

Our goal is to answer your needs at best, ethically, and in a cost-effective manner.

CC-plaquette-EN-3 CC-plaquette-EN-3

CC-plaquette-EN-3  CC-plaquette-EN-3

COPYRIGHT © 2011 -
Agence de communcation B.carré

Clinical research Consultants is a clinical and regulatory affairs CRO, based in central Paris, with activities throughout EU, US, Asia and the Middle East. CC Clinical research Consultants is particularly focused on compliance to moral, legal and scientific integrity. The company ensures full compliance with GCPs, ethical, legal and regulatory requirements governing the conduct of clinical research worldwide.