Strategic Advice and Regulatory Analysis

BlueReg experienced consultants can provide insight into all regulatory requirements for France:

  • Drug Registration
  • Early Access Programmes
  • Post Marketing Authorisation Application (MAA) activities
  • Promotional material review
  • Quality systems and audits
  • Interactions with healthcare professionals includingcompliance with the French laws (DMOS, Transparence de liens, Charte de l’information promotionnelle)
  • Pharmacovigilance
  • Pricing and reimbursement

Our experts

Associated News

The French system for preventing and managing shortages

The French regulation on the prevention and management of stock shortages of medicinal products is...

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New Appointment to our Leadership Team !

BlueReg Group is delighted to announce the appointment of Dominique Patrone as General Manager of PharmaBlue....

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Corinne Schmitz – Women for Future – Pharmaceutical Industry Expert

This week, “La Tribune” and its partner Bpifrance have decided to present Corinne Schmitz, CEO...

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