A dedicated team of highly qualified consultants providing services in France. The team have:

  • Significant hands-on industry experience and broad expertise in national Regulatory Affairs, Quality Management, Market Access and Pharmacovigilance.
  • Varied and flexible skills, ranging from strategic consulting to operational execution, as well as leading and managing projects.


This team provides expert advice as well as supporting with hands-on operational activities. The team works with many clients, from biotech start-ups to large pharma companies looking for local expertise or specific services for France. The team have a highly successful track record of delivering all projects, from the simple to the complex.

Our Latest Engagements


  • Review and submission of local promotional materials for pharmaceutical products and medical devices
  • Preparation of cohort ATU (early access) applications for an Orphan Drug
  • Handling of all local regulatory activities for a portfolio of pharmaceutical products
  • Supporting a US client in obtaining an “Exploitant” status from the French National Agency for the Safety of Medicines and Health Products (ANSM) for their newly created affiliate in France. This included providing strategic advice to the client, setting up a specific Quality Management System (QMS) and preparing the “Exploitant” application filed to ANSM.

Our experts

Associated News


BlueReg continues to monitor the changes in the regulatory guidance and we wish to share...

Learn more

How antibody testing can help us fight COVID-19 ?

There is a high demand around the need for antibody testing and the media frenzy...

Learn more

BlueReg continues to expand in the US opening its second North American office in Boston

Cambridge, Massachusetts, USA, December 13 2019, BlueReg, the consulting organization for life sciences companies, is...

Learn more