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A clinical research associate (CRA), also called a clinical monitor or trial monitor, is a health-care professional who performs many activities related to medical research, particularly clinical trials. Clinical research associates work in various settings, such as pharmaceutical companies, medical research institutes and government agencies.
Regulatory documents can be huge and are formulaic. They include clinical study protocols, clinical study reports, patient informed consent forms, investigator brochures and summary documents (e.g. in Common Technical Document [CTD] format) that summarize and discuss the data a company gathers in the course of developing a medical product.
Clinical officer is a professional designation established by the government through the Clinical Officers Council (COC) which has jurisdiction and responsibility for the clinical officer's training, registration and licensing and each officer must (1) study clinical medicine and surgery or clinical medicine and community health for three or ...
Caspard Consultants, a Paris-based contract research organization, and; Sitebase Clinical Systems, Inc., a provider of remote data entry technology designed to enhance the quality and timeliness of clinical trial data. [13] August 1996: Parexel acquires in separate transactions for a combined 1,008,304 own shares of common stock:
Fortrea Holdings Inc. is a contract research organization organized in Delaware and headquartered in Durham, North Carolina with operations in 90 countries. Its customers are primarily in the pharmaceutical, biotechnology, and medical device industries.
2000: ICON acquired UK-based regulatory consultancy, YRCR Ltd.; Central Laboratory in New York; and bioanalytical consultancy, Pacific Research [17] [18] [19] 2002: ICON acquired clinical research provider, BPA. [20] 2003: ICON acquired Medeval, a UK-based Phase I facility, and US consulting firm, Globomax [21] [22]
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