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  2. Royal Pharmaceutical Society - Wikipedia

    en.wikipedia.org/wiki/Royal_Pharmaceutical_Society

    The Royal Pharmaceutical Society of Great Britain had a museum collection since 1842, which continues to be managed by the RPS at its offices in East Smithfield. A historical collection was established in 1937 and expanded in the 1940s–1960s by Agnes Lothian . [ 10 ]

  3. Clinical governance - Wikipedia

    en.wikipedia.org/wiki/Clinical_governance

    Clinical governance is a systematic approach to maintaining and improving the quality of patient care within the National Health Service (NHS) and private sector health care. Clinical governance became important in health care after the Bristol heart scandal in 1995, during which an anaesthetist, Dr Stephen Bolsin , exposed the high mortality ...

  4. Regulated Product Submissions - Wikipedia

    en.wikipedia.org/wiki/Regulated_Product_Submissions

    Regulated Product Submission (RPS) is a Health Level Seven (HL7) standard designed to facilitate the processing and review of regulated product information. [1] RPS is being developed in response to performance goals that the U.S. Food and Drug Administration (FDA) is to achieve by 2012, as outlined in the Prescription Drug User Fee Act (PDUFA). [2]

  5. Clinical audit - Wikipedia

    en.wikipedia.org/wiki/Clinical_audit

    Swage T.; Clinical governance in health care practice. Oxford: Butterworth-Heinemann, 2000; Clinical Governance Support Team, A Practical Handbook for Clinical Audit. 2004; Clinical governance and re-validation: the role of clinical audit, Education in Pathology. 2002;117:47–50; The New NHS, Modern, Dependable, London: HMSO, 1997, ISBN 0-10 ...

  6. International Council for Harmonisation of Technical ...

    en.wikipedia.org/wiki/International_Council_for...

    In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.

  7. Good clinical practice - Wikipedia

    en.wikipedia.org/wiki/Good_clinical_practice

    A similar guideline for clinical trials of medical devices is the international standard ISO 14155, which is valid in the European Union as a harmonized standard. These standards for clinical trials are sometimes referred to as ICH-GCP or ISO-GCP to differentiate between the two and the lowest grade of recommendation in clinical guidelines.

  8. List of abbreviations for medical organisations and personnel

    en.wikipedia.org/wiki/List_of_abbreviations_for...

    National accrediting agency for clinical laboratory science: NAPCRG: North American Primary Care Research Group: NCA: National credentialing agency for laboratory personnel: NCI: National Cancer Institute NCTMB: Nationally certified in therapeutic massage and bodywork NEJM: New England Journal of Medicine: NHC: Nephrology Hypertension Clinic, P ...

  9. Medical guideline - Wikipedia

    en.wikipedia.org/wiki/Medical_guideline

    Plates vi & vii of the Edwin Smith Papyrus (around the 17th century BC), among the earliest medical guidelines. A medical guideline (also called a clinical guideline, standard treatment guideline, or clinical practice guideline) is a document with the aim of guiding decisions and criteria regarding diagnosis, management, and treatment in specific areas of healthcare.