- Clinical Trial Protocol
- Медицина: протокол клинического исследования
Универсальный англо-русский словарь. Академик.ру. 2011.
Универсальный англо-русский словарь. Академик.ру. 2011.
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 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 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 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
Clinical research — is a branch of medical science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving… … Wikipedia
Clinical trials unit — Clinical trials units (CTU) are specialised biomedical research units which design, centrally coordinate and analyse clinical trials and other studies. Some CTUs specialise in different methodologies, such as randomised controlled trials, cluster … 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
Protocol — may also refer to:Standards in information automation: * Communications protocol * Protocol (computing) * Protocol (object oriented programming) * Cryptographic protocolProcedures for human behavior: * Protocol (diplomacy) * Protocol, a.k.a.… … 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