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  2. Clinical endpoint - Wikipedia

    en.wikipedia.org/wiki/Clinical_endpoint

    Clinical endpoint. Clinical endpoints or clinical outcomes are outcome measures referring to occurrence of disease, symptom, sign or laboratory abnormality constituting a target outcome in clinical research trials. The term may also refer to any disease or sign that strongly motivates withdrawal of an individual or entity from the trial, then ...

  3. Contract research organization - Wikipedia

    en.wikipedia.org/wiki/Contract_research_organization

    Contract research organization. In the life sciences, a contract research organization ( CRO) is a company that provides support to the pharmaceutical, biotechnology, and medical device industries in the form of research services outsourced on a contract basis. A CRO may provide such services as biopharmaceutical development, biological assay ...

  4. Clinical data repository - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_repository

    Clinical data repository. A Clinical Data Repository (CDR) or Clinical Data Warehouse (CDW) is a real time database that consolidates data from a variety of clinical sources to present a unified view of a single patient. It is optimized to allow clinicians to retrieve data for a single patient rather than to identify a population of patients ...

  5. Clinical decision support system - Wikipedia

    en.wikipedia.org/wiki/Clinical_decision_support...

    Clinical decision support system. A clinical decision support system ( CDSS) is a health information technology that provides clinicians, staff, patients, and other individuals with knowledge and person-specific information to help health and health care. CDSS encompasses a variety of tools to enhance decision-making in the clinical workflow.

  6. Registration, Evaluation, Authorisation and Restriction of ...

    en.wikipedia.org/wiki/Registration,_Evaluation...

    C294, 25.11.2005, pp. 38–44. Registration, Evaluation, Authorisation and Restriction of Chemicals ( REACH) is a European Union regulation dating from 18 December 2006. [1] REACH addresses the production and use of chemical substances, and their potential impacts on both human health and the environment. Its 849 pages took seven years to pass ...

  7. Clinical neurophysiology - Wikipedia

    en.wikipedia.org/wiki/Clinical_neurophysiology

    Clinical neurophysiology. Clinical neurophysiology is a medical specialty that studies the central and peripheral nervous systems through the recording of bioelectrical activity, whether spontaneous or stimulated. It encompasses both research regarding the pathophysiology along with clinical methods used to diagnose diseases involving both ...

  8. Health informatics tools - Wikipedia

    en.wikipedia.org/wiki/Health_informatics_tools

    Tools. Front-line health informatics tools (sometimes informally called the " clinical informatics toolbelt ") generally include one of the following: Policies and procedures – Tools used to define organizational standards and how to achieve them. Clinical protocols – Tools used to standardize and automate care in a common clinical scenario.

  9. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    A trial master file contains essential documents for a clinical trial that may be subject to regulatory agency oversight. In the European Union (EU), TMFs have a different definition and set of requirements than in the US. The EU Commission's Directive 2005/28/EC 63 Chapter 4 states 'the trial master file shall consist of essential documents ...

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