Business

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.

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

Company in Germany specialized in contract research and custom synthesis of active pharmaceutical ingredients as well as chemical specialties in small quantities.

CTS software manufacturer for clinical trials support and documentation of patient medical files.

Contract research clinical CRO, operating worldwide. Provides information about clinical trial support services and associated expertise.

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

Provides clinical research services to pharmaceutical, medical devices, and cosmetics industries. Information about company structure, ongoing clinical trials and regulatory adherence to the ICH GCP guidelines.

Offers full service preparation of clinical trial materials for phase I-IV studies into human and veterinary drugs. Features details of each stage. St Gely du Fesc, France.

Provides assistance with study conception, biometry, monitoring, and audit. Includes details of certification and specificity. Rueil-Malmaison, France.

Provides site and investigator identification, monitoring, regulatory board and ethics committee clearances, customs clearance and clinical trial logistics.

Provides data management, biometrics and medical writing for phase I-IV clinical studies and expert scientific consulting.

Conducting Phase 1 through Phase 4 multinational clinical studies. Facilities include three specialized Phase 1 clinical pharmacology units and bioanalytical laboratories.

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.

Offers complete clinical research programs or a modular approach involving monitoring, data management or biometrics. Based in Germany. [English and German]

Provides design, setup, and conduct of clinical trials, including large Phase II and III international studies involving hundreds of patients. Operating in Central Europe, Russia, and other CIS countries.

Provides phase I-IV clinical research services throughout Europe. Offers all clinical trial services, data management, statistics, medical writing, project managing, monitoring and GCP auditing.

Providing consultancy to the pharmaceutical and biopharmaceutical industry: medical writing (IBs, preclinical and clinical reports, publications), datamanagement (CRF, double encoding), biostatistics (sample size, RAP, reports)and regulatory affairs.

Site management organisation (SMO) with ten professional, dedicated investigation sites, exclusively focused on patient recruitment for clinical trials in the UK.

Manages phase II-IV clinical trials and offers services for post-marketing surveillance, quality assurance auditing, biometrics, medical writing and medical device trials and registration. Germany.