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CRO based in Germany operates clinical pharmacology research units, including a sleep lab, and provides multicenter trials management, medical writing, data management, biostatistics, psychometrics and psychophysiology, and consulting services

A Paris-based CRO providing monitoring, data management, biostatistics, clinical writing and project management services to the pharmaceutical industry.

Clinical and bioanalytical contract research specialized in phase I, phase II and proof of concept studies for the pharmaceutical and cosmetic industries. Headquartered in France.

Provides clinical data management, statistics and reporting quality services to the pharmaceutical industry. Also offers specialised recruitment service in the clinical trials arena, providing staff as an interim management project or direct recruitment into your organisation.

Providing support to the pharmaceutical industry by conducting clinical trials to determine safety, tolerance, and efficacy in Belfast, North Ireland

Provides a wide range of services including clinical pharmacology phase I studies in its two research centres in Rennes and Paris (more than 100 beds total), multinational clinical trials and preclinical pharmacology.

Executes classical phase 1 trials in Belgium in which pharmacokinetics, drug interactions, tolerability and safety of compounds are evaluated in healthy volunteers.

European CRO headquartered in the Czech Republic conducts Phase I-IV clinical trials, bioavailability and bioequivalence studies, and offers bioanalytical and statistical services.

A European full service clinical contract research organisation offering clinical monitoring, data management, statistical consulting and programming, and medical writing.

Offers clinical trial services and consulting for phase 1 through phase 4 trials in Central Europe.