Cebiphar CRO

Cebiphar, analytical CRO for Life Sciences product development since 1979, provides technical and regulatory compliant solutions to secure our clients supply chain

As a service provider, we support and advise healthcare industries in solving their problems at every stage of product development in France and abroad.

Services Our expertise

CEBIPHAR fits to your needs

Every customer is unique and each project is different: CEBIPHAR’s teams are very attentive to proposing relevant solutions suitable to the background of your project.

Whether your projects are linked to analytical development, release control, or support for regulatory variations, CEBIPHAR always involves skilled people. CEBIPHAR’s ability to adapt its organization specifically to your project is definitely a key selection criteria within our customers portfolio.

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Thematic tool

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Accueil Cycle de Vie Cebiphar

Analytical method Life Cycle tool

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Latest News

Find the latest news about CEBIPHAR and TERANGA Groupe companies, as well as news related to the Life Sciences industry

CEBIPHAR updates

CPhI : The leading event for the pharmaceutical industry is back!

Bringing together thousands of providers and players from the pharmaceutical industry across the supply chain, CPhI Worldwide is the best platform to search for...
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CEBIPHAR updates


As part of our sustainable customer experience program, a customer satisfaction survey was conducted in June 2021, aiming to build long-term relationships with our...
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Our news on LinkedIn

Nous sommes fiers de partager avec vous le chemin parcouru deux ans après le lancement du site CEBIPHAR Toulouse:

Nous avons obtenu le statut d’établissement pharmaceutique et nos équipes se sont agrandies. (…) Ces quelques mots de notre directeur de site à Toulouse lors d’une interview donnée à Toulouse Métropole en Juillet 2020

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Fully committed to Quality

Our quality standards: GMP – Good Manufacturing Practices, GMP applicable in France, GMP applicable in the European Union [Eudralex Volume 4], cGMP applicable in the United States [CFR21 part 210 & 211]

Our certifications as a human and veterinary pharmaceutical company:

  • Pharmaceutical establishment approved by ANSM since 2001 on Fondettes site (Human medicinal products and Human Investigational Medicinal Products) and since 2020 on Toulouse site. Last inspection in May 2019: quality control of human drugs, experimental drugs and imported drugs
  • Pharmaceutical establishment approved by ANSES since 2005 on Fondettes site and since 2020 on Toulouse site. Last inspection in March 2021:quality control of veterinary drugs and veterinary drugs subjected to clinical trials
  • Site inspected by FDA (last inspection: September 2017)
  • Certificate of conformity to GLP (ANSES) since 2000 for Fondettes site. Last inspection in March 2021.
  • VICH GL9: good clinical practice for veterinary medicinal products
  • CEBIPHAR is also CIR (Crédit Impôt Recherche) accredited
THE UNION OF 3 ENTITIES A strong link between TERANGA Groupe companies offers you a broad range of services

The independent holding company TERANGA combines the synergy of a group with the flexibility of companies on a human scale. 

Offering complementary services and experiences, ACM Pharma, CEBIPHAR and UPS Consultants form a leading group dedicated to the human and veterinary healthcare and cosmetic industries throughout Europe.

These expertises are expressed in the fields of product development, technical, regulatory support, quality control, microbiology with the concern to ensure the reliability and quality of the data.

Learn more about Teranga Groupe

Your partner specialized in contamination control.

ACM Pharma

Your personalized support for the development and control of your health products.

UPS Consultants

For more than 20 years, it has been developing its intervention capacities for training, consulting, auditing and technical assistance missions.


The main objective of our Newsletter is to focus on one of our services by showing the added value it can bring you.

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