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This category is for listing of contract research organizations that are based in Europe and conduct clinical trials primarily in Europe
Company in Germany specialized in contract research and custom synthesis of active pharmaceutical ingredients as well as chemical specialties in small quantities.
Offers complete clinical research programs or a modular approach involving monitoring, data management or biometrics. Based in Germany. [English and German]
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.
Bio-Kinetic Europe, Ltd.
Providing support to the pharmaceutical industry by conducting clinical trials to determine safety, tolerance, and efficacy in Belfast, North Ireland
Headquartered in the Czech Republic, conducts Phase I-IV clinical trials, bioavailability and bioequivalence studies, and offers bioanalytical and statistical services.
Based in Hungary and providing clinical trial services, statistical analysis, medical writing, clinical quality assurance and assessment of cost-effectiveness.
Dr. M. Koehler GmbH
Providing support to pharmaceutical industry and medical research in design, conduct, analysis and data management in their clinical trials.
Providing monitoring, data management, biostatistics, clinical writing and project management services. Paris, France.
Services include project feasibility analysis, site selection, site initiation, monitoring, audits and project closure. Hungary.
Planning and implementing post-marketing surveillance studies.
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.
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.
Offers a range of services, including data management, statistics, and medical writing, to the pharmaceutical industry, and other services through strategic partnerships.
Resourcing solutions for the pharmaceutical industry with a focus on clinical development and medical affairs.
Specializing in the implementation and management of clinical trials in Poland.
Headquartered in Mannheim, Germany and offers services such as phase II/III clinical studies, medical writing/publishing, drug safety affairs, MedDRA coding, data management.
K.A. Seldeslagh & Associates (Kasa)
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.
Offers clinical trial services and consulting for phase 1 through phase 4 trials in Central Europe.
Provides assistance with study conception, biometry, monitoring, and audit. Includes details of certification and specificity. Rueil-Malmaison, France.
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.
Winicker Norimed GmbH
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.
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.
Site management organisation (SMO) with ten professional, dedicated investigation sites, exclusively focused on patient recruitment for clinical trials in the UK.
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.
GC Clinical Trials
Provides site and investigator identification, monitoring, regulatory board and ethics committee clearances, customs clearance and clinical trial logistics.
Clinical CRO offers all phases of clinical trials and registry projects. Provides information about study planning, clinical data management, and previous clinical study experience. Located in Freiburg, Germany.
Contract research clinical CRO, operating worldwide. Provides information about clinical trial support services and associated expertise.
Clinical trial support CRO with mathematical and biostatistic analysis focus. Provides eCFR web-based services, patient registry, CRM, and CTMS services.
Network of european brain and tissue banks for clinical and basic science research. Provides information on the biology of brain disease.
Provides health technology assessment consulting for the pharmaceutical industry, offers CRO services in epidemiology, data analysis and evidence synthesis fields.