clinical study site

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• Clinical study design — is the formulation of trials and experiments in medical and epidemiological research, sometimes known as clinical trials. Many of the considerations here are shared under the more general topic of design of experiments but there can be others, in …   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 Trial Portal — Not to be confused with Clinical Trials Registry or Clinical Trial Management System. A clinical trial portal (also known as clinical portal or clinical study portal) is a web portal or enterprise portal that primarily serves sponsors and… …   Wikipedia

• Clinical data management system — A clinical data management system or CDMS is a tool used in clinical research to manage the data of a clinical trial. The clinical trial data gathered at the investigator site in the case report form are stored in the CDMS. To reduce the… …   Wikipedia

• 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

• Clinical death — is the medical term for cessation of blood circulation and breathing, the two necessary criteria to sustain life.[1] It occurs when the heart stops beating in a regular rhythm, a condition called cardiac arrest. The term is also sometimes used in …   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 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

• 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

• 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 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