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.

Providing monitoring, data management, biostatistics, clinical writing and project management services. Paris, France.

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.

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.

Based in Hungary and providing clinical trial services, statistical analysis, medical writing, clinical quality assurance and assessment of cost-effectiveness.

Provides phase II-IV clinical trials conduct and management in the Northwest of England, specializing in mental health disorders.

Designs and conducts clinical studies and also prepares marketing for drugs, cosmetics, dietetic products and medical devices. Features details of each stage and directions to facility. 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.

Providing support to pharmaceutical industry and medical research in design, conduct, analysis and data management in their clinical trials.

Performs clinical and post marketing surveillance trials using an internet-based electronic data capture (EDC) system.

Offers design of antisense design, target validation, consultancy, experimental services. Includes product information, overview of applications and company in Midlothian, Scotland.

Based in Germany and offering clinical development services, including a phase I unit with laboratory and data management services.

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

Services include project feasibility analysis, site selection, site initiation, monitoring, audits and project closure. Hungary.

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.

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.

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

Offers project management and staff resourcing services. United Kingdom.

Specializing in the implementation and management of clinical trials in Poland.

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.

Based in Switzerland and Germany and offering services in clinical research, regulatory affairs and training programs.

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. Germany.

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.

Offers phase I and II clinical research and testing in a state-of-the-art 57-bed facility in the United Kingdom.

Planning and implementing post-marketing surveillance studies.

Operating in Central Europe, Russia, and other CIS (Commonwealth of Independent States) countries. Provides design, setup, and conduct of clinical trials, particularly large Phase II and III international studies involving hundreds of patients all across the CIS.

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.

Offers comprehensive management of clinical trials in Scandinavia and the Baltic states.

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.

Danish company located in Medicon Valley, Denmark offers professional freelance nursing assistance to investigators in Europe for faster recruitment and higher quality of data.

Offering data management, biostatistics, medical writing, monitoring and other services needed to plan, initiate, conduct and report clinical trials.

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.

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.