Organizations providing services in clinical trials site management.


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Gulf Coast Research Associates

Site management organization (SMO) specializing in conducting outpatient and inpatient phase II-IV clinical trials involving pharmaceutical, biological and medical device products.




MedFocus

Services in data management, SAS programming, biostatistics, clinical site monitoring and clinical project management.




NHMRC Clinical Trials Centre

Specializing in clinical trials research in Australia, coordinating its own and assisting others in conducting large-scale, multi-centre clinical trials.




PharmaLinkFHI

Experience in clinical research management in over 100 countries around the world.




PharmaNet

International contract research organization offering services related to clinical trials including data management, biostatistics, regulatory affairs, study monitoring, site management and protocol design.




Precision Research, Inc.

Services in clinical trials management, medical writing, study site monitoring, and plan design.




Primary Care Research Center

Expanded our clinical research services and resources and can serve as a Site Management Organization coordinating research projects in multiple Primary Care and Specialist offices in the Northern Virginia (DC suburban) area.




SMO-USA, Inc.

A Site Management Organization whose sole purpose is to support the successful outcome of clinical trials for the pharmaceutical, biotechnology, and medical device industries.




University of Hong Kong - Clinical Trials Centre

Coordinates and advises on the preparation and design of protocols, pre-study statistical requirements, budgeting and writing.




USCardioVascular

Company for the development of outpatient cardiovascular diagnostic facilities for physician groups and hospitals.




Tips & Advice to help you make your decision on Clinical Drug Trial Site Management

Clinical drug trial site management involves the supervision of a clinical drug trial from start to finish. A clinical drug trial manager must oversee the recruitment of patients and doctors, regulatory compliance, site initiation, and collection of data. Clinical trials typically include three phases, each with a larger pool of participants and research scope than the last. All three clinical trials must be completed before the U.S. Food and Drug Administration will approve a new drug.

If your pharmaceutical or biotechnology company is unable to handle clinical drug trial site management on its own, you can hire a clinical trial management company to do this work for you. ... more


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