- Clinical Research Organization
- Фармация: клиническая исследовательская организация
Универсальный англо-русский словарь. Академик.ру. 2011.
Clinical Research Organization
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Clinical research organization — The Clinical Research Organization (CRO), also known as a contract research organization, is an independent organization involved in the conduct of a clinical trial. A CRO is responsible for the Data Management (DM) and the communication between… … Wikipedia
Contract research organization — A contract research organization, also called a clinical research organization, (CRO) is a service organization that provides support to the pharmaceutical and biotechnology industries in the form of outsourced pharmaceutical research services… … Wikipedia
Clinical research associate — A clinical research associate (CRA) is a profession defined by Good clinical practice guidelines (ICH GCP). The main function of a clinical research associate is to monitor clinical trials. He or she may work directly with the sponsor company of… … Wikipedia
List of clinical research topics — Clinical research is the aspect of biomedical research that addresses the assessment of new pharmaceutical and biological drugs, medical devices and vaccines in humans. Contents 1 General topics 2 Drug terminology 3 T … Wikipedia
Community Programs for Clinical Research on AIDS — CPCRA, the Community Programs for Clinical Research on AIDS, is according to their own website: an experienced community based clinical trials network whose main goal is to obtain evidence to properly inform healthcare providers and people living … Wikipedia
Clinical trial — Clinical trials are a set of procedures in medical research and drug development that are conducted to allow safety (or more specifically, information about adverse drug reactions and adverse effects of other treatments) and efficacy data to be… … Wikipedia
Clinical Data Interchange Standards Consortium — (CDISC) is a non profit organization, whose mission is to develop and support global, platform independent data standards that enable information system interoperability to improve medical research and related areas of health care . Their main… … Wikipedia
Clinical trial protocol — Clinical protocol redirects here. For clinical guidelines not involving trials, see Medical guideline. A clinical trial protocol is a document that describes the objective(s), design, methodology, statistical considerations, and organization of a … Wikipedia
Clinical trials publication — is having research published in a peer reviewed journal following clinical trials. Most investigators will want to have such a publication but the nature of clinical trials may create special considerations and obstacles. Most agreements for a… … Wikipedia
Clinical trials registry — A clinical trials registry, sometimes abbreviated as a CTR, is an official platform and catalog for registering a clinical trial. Some countries require clinical trials being conducted in that country to be registered, other do not require it,… … Wikipedia
Clinical trial management — A clinical trial is the application of the scientific method to human health. Since such trials require the use of human test subjects and can severely impact the well being of the subjects, as well as treatments of other people and large amounts … Wikipedia
