clinical trial site

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• 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 — 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 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

• Site management organization — (SMO) could refer to an individual, a network of individuals or an organization that sub contracts clinical trial related responsibilities from a contract research organization (CRO). Some, but not all responsibilities could include:* Contract… …   Wikipedia

• Clinical — can refer to: Clinical (or bedside) medical practice, based on observation and treatment of patients as opposed to theory or basic science Clinic Illness, a state of poor health Clinical chemistry, the analysis of bodily fluids Clinical… …   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 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 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

• Clinical site — A clinical site is a medical facility staffed with a clinical investigator (MD) and qualified for performing clinical research. To be qualified as a clinical site, strict regulations are to be adhered to. The foundations for these regulations are …   Wikipedia