English-Russian glossary of clinical practice. 2002.
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
Monitoring in clinical trials — Clinical monitoring Oversight and administrative efforts that monitor a participant s health during a clinical trial. The government and other clinical trial funding agencies require data and safety monitoring boards to oversee clinical trials.… … 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
Glossary of clinical trials — A glossary of terms used in clinical trials. NOTOC CompactTOC8 side = yes refs = yes A * Activities of daily living:: The tasks of everyday life. These activities include eating, dressing, getting into or out of a bed or chair, taking a bath or… … Wikipedia
Clinical data acquisition — Acquisition or collection of clinical trial data can be achieved through various methods that may include, but are not limited to, any of the following: paper or electronic medical records, paper forms completed at a site, interactive voice… … Wikipedia
Clinical decision support system — (CDSS or CDS) is an interactive decision support system (DSS) Computer Software, which is designed to assist physicians and other health professionals with decision making tasks, as determining diagnosis of patient data. A working definition has… … 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 data management — encompasses the entry, verification, validation and quality control of data gathered during the conduct of a clinical trial. Contents 1 Role of the Clinical Data Manager in a Clinical Trial 2 Standard Operating Procedures 3 The Data Management… … 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
Clinical research coordinator — The Clinical Research Coordinator (CRC) is responsible for conducting clinical trials using good clinical practice [1] (GCP) under the auspices of the Principal Investigator (PI). Good Clinical Practices Principles have been defined by Madelene… … 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
