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Clinical Research Information System

См. также в других словарях:

  • Clinical Care Classification System — The Clinical Care Classification (CCC) System is a standardized, coded nursing terminology that identifies the discrete elements of nursing practice. The CCC provides a unique framework and coding structure for documenting the plan of care… …   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 management system — A Clinical Trial Management System, also known as CTMS, is a customizable software system used by the biotechnology and pharmaceutical industries to manage the large amounts of data involved with the operation of a clinical trial. It maintains… …   Wikipedia

  • Clinical Trial Management System — A Clinical Trial Management System, also known as CTMS , is a customizeable software system used by the biotechnology and pharmaceutical industries to manage the large amounts of data involved with the operation of a clinical trial. It maintains… …   Wikipedia

  • Hospital information system — There are various titles and acronyms which all declare similar approaches to managing the information flow and storage in hospital routine services, as Hospital Information System (HIS), or Healthcare Information System, or Clinical Information… …   Wikipedia

  • Laboratory information system — A lab information system (LIS), is a class of software which handles receiving, processing and storing information generated by medical laboratory processes. These systems often must interface with instruments and other information systems such… …   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 — 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 audit — is a process that has been defined as a quality improvement process that seeks to improve patient care and outcomes through systematic review of care against explicit criteria and the implementation of change .[1] The key component of clinical… …   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 surveillance — (or Syndromic surveillance) refers to the surveillance of health data about a clinical syndrome that has a significant impact on public health, which is then used to drive decisions about health policy and health education. This is distinct from… …   Wikipedia

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