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Experienced conducting studies for international and domestic programs in Phases I - IV. Diverse therapeutic expertise gathered over 10 years can be applied to both single and full service projects.

German CRO provides data management, biometrics and medical writing for phase I-IV clinical studies and expert scientific consulting for CNS programs.

A mid-size European focused CRO conducting Phase 1 through Phase 4 multinational clinical studies for the pharmaceutical industry. Facilities include three specialized Phase 1 clinical pharmacology units and bioanalytical laboratories.

Headquartered in Mannheim, Germany and offers services such as phase II/III clinical studies, medical writing/publishing, drug safety affairs, MedDRA coding, data management.

Provides clinical, regulatory, marketing, training and authorized representative services to medical device, pharmaceutical and biotechnology companies to facilitate market introduction in Europe and continuing compliance of new and existing products.

Provides medical data management, monitoring, analysis, medical and statistical expert reports, consultancy and biometrical expertises for international pharmaceutical research companies.

Provides biostatistical and epidemiological consultancy in clinical trials and other medical research projects. Expertise in multivariate statistical analysis, survival analysis, factor analysis, meta-analysis, multi-level modeling and other advanced statistical analysis.

Provides initiation and management of medical research projects for medical drugs and devices and also regulatory consultancy and filings

A full-service Scandinavian contract research organisation CRO) headquartered in Denmark.

A "not-for-profit" CRO based in the UK contracting to the pharmaceutical and biotech industry offers project management and staff resourcing services.