Cebiphar offers a wide range of services in the field of health products development. Taking advantage of our state of the art technical platform, located on 2 strategic sites, in Fondettes near Tours and Pessac near Bordeaux, our teams of pharmacists, engineers, chemists, biologists, veterinary doctors and technicians provide services with utmost care and quality to R&D and control laboratories, as well as regulatory departments of human and veterinary pharmaceutical industry.

A 30-year experience in pharmaceutical development

Cebiphar has performed studies for over 1.600 pharmaceutical products, hence building a strong and extensive know-how in health products development. Combining a technical and regulatory experience, Cebiphar provides a complete service offer including:

• Consulting and expertise,
• Formulation and analytical development,
• Stability studies,
• Quality control analysis,
• Veterinary pre-clinical and clinical studies
• All associated regulatory services.

Our commitment to quality and service

Cebiphar performs its studies in strict compliance with the most up-to-date quality standards, GMP, cGMP, GLP, GCP and has obtained the following authorisations from the French health authorities:

• GMP compliant Pharmaceutical site (AFSSAPS)
• GMP compliant Pharmaceutical site (AFSSA)
• GLP compliant test site (AFSSA)

Cebiphar is also a trusted partner to the world's leading pharmaceutical companies. It benefits from the renewed confidence of more than 150 clients. Definitely customer-focused, Cebiphar has the permanent objective to provide the most cost and time-efficient solutions, in strict compliance with current quality standards.