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Professional full-service CRO, operating in Russia and former USSR countries. Specializing in 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.

A leading Danish CRO offering data management, biostatistics, medical writing, monitoring and all 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.

A German CRO which manages Phase II-IV clinical trials and also offers services for post-marketing surveillance, quality assurance auditing, biometrics, medical writing and medical device trials and registration.