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  2. Clinical quality management system - Wikipedia

    en.wikipedia.org/wiki/Clinical_Quality...

    Clinical quality management systems (CQMS) are systems used in the life sciences sector (primarily in the pharmaceutical, biologics and medical device industries) designed to manage quality management best practices throughout clinical research and clinical study management. A CQMS system is designed to manage all of the documents, activities ...

  3. National Institutes of Health Clinical Research Training Program

    en.wikipedia.org/wiki/National_Institutes_of...

    A number of one-year research training programs have arisen in the US, including the Howard Hughes Medical Institute (HHMI) Medical Fellows Program (1984–present), the HHMI-NIH Research Scholars Program (1989–present), the Doris Duke Clinical Research Fellowship Program, and the Sarnoff Cardiovascular Foundation Research Fellowship Program.

  4. Standard operating procedure - Wikipedia

    en.wikipedia.org/wiki/Standard_operating_procedure

    A standard operating procedure (SOP) is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations. [1] SOPs aim to achieve efficiency, quality output, and uniformity of performance, while reducing miscommunication and failure to comply with industry regulations .

  5. Site management organization - Wikipedia

    en.wikipedia.org/wiki/Site_management_organization

    A Site Management Organization (SMO) is an organization that provides clinical trial-related services to a contract research organization (CRO), a pharmaceutical company, a biotechnology company, a medical device company, or a clinical site.

  6. Clinical data management - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management

    Clinical data management (CDM) is a critical process in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials. [1] Clinical data management ensures collection, integration and availability of data at appropriate quality and cost.

  7. Protocol (science) - Wikipedia

    en.wikipedia.org/wiki/Protocol_(science)

    A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study. While in a clinical trial, participants following a protocol are seen regularly by research staff to monitor their health and to determine the safety and effectiveness of their treatment.

  8. Clinical pathway - Wikipedia

    en.wikipedia.org/wiki/Clinical_pathway

    The clinical pathway concept appeared for the first time at the New England Medical Center (Boston, United States) in 1985, inspired by Karen Zander and Kathleen Bower. [9] [non-primary source needed] Clinical pathways appeared as a result of the adaptation of the documents used in industrial quality management, the standard operating procedures (SOPs), whose goals are:

  9. Canadian Science Centre for Human and Animal Health

    en.wikipedia.org/wiki/Canadian_Science_Centre...

    Extensive Standard operating procedures (SOPs) are in place and everyone is well-trained for the specific area they work in. A safety and environmental services (SES) team provides numerous "hands-on" demonstrations and presentations on biosafety and occupational health and safety throughout the year and provides 24/7 response to biological or ...

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