Our team

Maurice

BAGOT d’ARC

Founder, General Director

ENT surgeon, head and neck surgeon, specialized in ENT oncology, legal compensation for bodily injury, and pharmaceutical marketing, with over 30 years of experience in Medical Affairs serving the healthcare industries and 15 years of surgical practice.

He has extensive experience in the pharmaceutical and medical device fields as an international medical director, focusing on market development, clinical trial management and publication planning, marketing, medical education, communication, and pharmacovigilance.

Claudia

DELIN

Project Manager, Quality Assurance Manager, and Professional Trainer

With 25 years of experience in Medical Affairs and Clinical Operations across various therapeutic areas (endocrinology, diabetes, surgery, interventional radiology…) and different organizations (pharmaceutical companies, CROs),

She supports healthcare industries and start-ups in managing clinical, observational, and epidemiological trials, developing medical writing strategies, and training personnel dedicated to the promotion of healthcare products. She holds a DESS (Diploma of Higher Specialized Studies) in Nutrition (USTL Montpellier) and a Specialized Master’s in Innovation Management and Technology Transfer (ESC Toulouse).

Sami

BEN ABDALLAH

Senior Clinical Research Associate, and Professional Trainer

Professional experience in scientific and medical communication, strategy and environment, medico-marketing, and professional training.

 

Holding a University Diploma in Clinical Research Associate (D.U. d’ARC), a Master’s degree in Research in Neurosciences, and a Master’s degree in Biotechnology, he participates in various stages of clinical research missions.

Our assets

Qualiopi Certificate

BluePharm has been certified Qualiopi since 2020.

ISO 9001-2015

BluePharm has been certified ISO 9001-2015 since 2022.

Research Tax Credit

BluePharm is approved Research Tax Credit.

As a dynamic company, BluePharm relies on valuable assets:

  • Over 25 years of experience in R&D,
  • Extensive knowledge in most surgical specialties,
  • Extensive knowledge in medical fields (infectious diseases, diabetology, cardiology, ENT),
  • Approval for the CIR (Research Tax Credit),
  • Qualiopi certification for professional training programs.

The quality assurance program in place at BluePharm is designed to ensure the best service for its clients and to conduct studies in compliance with:

  • Good Laboratory Practice (GLP),
  • Good Clinical Practice (GCP),
  • Good Clinical Laboratory Practice (GCLP),
  • And with international guidelines (FDA, EMA, PMDA, MDR, …) as well as local regulatory requirements.

Member of AFCROs

BluePharm is a CRO based in Paris, operating in France and internationally (Europe, Asia-Pacific, Americas), where it conducts 20% of its business.

Qualified staff

Thanks to a qualified staff with an average of 25 years of experience, stable and responsive, the quality of services provided by BluePharm is recognized and consistent, with a customer satisfaction rate close to 100%.

Building your projects

BluePharm has already worked with several companies, 87% of which continue to place their trust in us. This is a concrete, objective, and motivating factor that drives us to help you successfully carry out your projects.

Clinical trials

We have managed multiple phase II and III clinical trials during product development, phase IV studies during the launch phase, as well as non-interventional studies and registries.

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Présentation de BluePharm Academy : Les modules de formation de BluePharm