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 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.
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. Germany.
A European full service clinical contract research organisation offering clinical monitoring, data management, statistical consulting and programming, and medical writing.
Based in Hungary and providing clinical trial services, statistical analysis, medical writing, clinical quality assurance and assessment of cost-effectiveness.
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.
A full-service European contract research organisation based in the Netherlands providing clinical trials services to the pharmaceutical, biotechnology and medical device industries.
Swiss clinical research organization specializing in clinical research, regulatory services and medical marketing support for medical devices and in-vitro diagnostics.
Provides assistance with study conception, biometry, monitoring, and audit. Includes details of certification and specificity. Rueil-Malmaison, France.
Conducting Phase 1 through Phase 4 multinational clinical studies. 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.
Offers a range of services, including data management, statistics, and medical writing, to the pharmaceutical industry, and other services through strategic partnerships.
Providing a broad range of sophisticated services supporting clinical trial programs ranging from small studies to international megatrials, for a wide variety of indications, since 1984.
Performs safety and tolerance (including first in man), pharmacokinetic, bioavailability and bioequivalence trials in a 36 bed research facility in Mönchengladbach Germany.
Offers complete clinical research programs or a modular approach involving monitoring, data management or biometrics. Based in Germany. [English and German]
Founded in Zürich to promote therapy and prevention of disease by enabling pharmaceutical and biotechnology companies to develop and register products, medical devices, and functional food.
An independent research service institute. Provides testing and assessment of the human and environmental safety of products from pharmaceutical, chemical and biotechnology industries. Located in Switzerland.
Provides site and investigator identification, monitoring, regulatory board and ethics committee clearances, customs clearance and clinical trial logistics.
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.
A Scandinavian contract research organization based in Stockholm, Sweden. We perform clinical project management, data management and pharmacovigilance for international pharmaceutical and medical device companies.
Specializes in clinical trials, providing services in clinical pharmacology (owned clinical research unit), clinical research (phases II to IV), data management, statistics, consulting, and project management.
Site management organisation (SMO) with ten professional, dedicated investigation sites, exclusively focused on patient recruitment for clinical trials in the UK.
Strategic planning and medical education consultancy with experience in phase I and II product development and clinical trial management for urological disorders.
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.
