OPTIMED Clinical Research  is a Contract Research Organization (CRO), which offers its experience for phase I to phase IV studies and surveys.

Located in France, OPTIMED Clinical Research has led several hundreds of clinical studies on behalf of the pharmaceutical and agro-food industries, with the aid of :

• A 60-bed Clinical Pharmacology Unit for Phase I studies
• A 32-bed hospital based ClinPharm Unit in Lyon
• An experienced and stable clinical staff of physicians, study nurses, technicians and scientists.
• A monitoring team
• Data Management, Statistics and Medical Writing services

With its highly trained staff and up-to-date equipment, OPTIMED offers high standard quality services.

Making your constraints its own, we have set up an efficient organization for your studies : adherence to deadlines, cost control, and commitment to optimal quality.

Thanks to its experience, Optimed Clinical Research has developed expertise, in terms of organization, management, medical writing, regulatory management. Consequently, Optimed can support you at each step of your clinical trial.

In February 2006, Optimed joined the Eurofins group, worldwide leader in the bioanalytical testing market and in pharmaceutical services. This partnership allows Optimed to extend the range of services provided in drug development thanks to the synergy of the different companies of the group.

Optimed’s Strengths : Two Independent and well-sized Clinical Pharmacology Units, integrated into an international group  A complete range of services in drug development : toxicology, pharmaceutical control, bioanalysis, central laboratory Well-recognized expertise in early drug development Stable team with 20-years of experience An efficient recruitment policy for the best respect of time-lines

Optimed vision :  Our main concern VOLUNTEER SAFETY Our commitment QUALITY AND RELIABILITY OF COLLECTED DATA