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BlueReg Group Global Regulatory Affairs

Case studies

 - 

2 December 2020

Registration & maintenance activities for all product portofolio in Sub Saharian French Speaking Area (SSFSA)

A big pharmaceutical company entrusted BlueReg (BR) to assist its regulatory team in regulatory activities in SSFSA.

Case studies

 - 

18 February 2020

Global Regulatory Affairs (GRA) Outsourcing Platform

A global biopharmaceutical company entrusted to BlueReg the management of daily regulatory activities for a large portfolio of medicinal products in various therapeutic areas, the objective being to focus their internal resources on strategic projects. The outsourced activities encompassed development…

Brochure

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28 May 2019

Our brand new digital brochure is now available

  Discover all our services and how BlueReg can provide you with strategic regulatory advice and hands-on outsourcing solutions through the entire lifecycle of your products.

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Composed of proven experts from the pharmaceutical industry, our team is ready to answer to your needs in any area of product development, commercialisation and early access programs, and life cycle management

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Welcome to BlueReg, an international consulting company for the pharmaceutical industry, specializing in development, regulatory affairs, economic affairs, quality and pharmacovigilance. We have built long-term partnerships with many clients by offering them “tailor-made” services guaranteeing expert advice and efficient solutions, thus supporting their projects towards success.

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