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  2. Good manufacturing practice - Wikipedia

    en.wikipedia.org/wiki/Good_manufacturing_practice

    Current good manufacturing practices (cGMP) are those conforming to the guidelines recommended by relevant agencies. Those agencies control the authorization and licensing of the manufacture and sale of food and beverages , [ 1 ] cosmetics , [ 2 ] pharmaceutical products , [ 3 ] dietary supplements , [ 4 ] and medical devices . [ 5 ]

  3. List of government agencies of Nepal - Wikipedia

    en.wikipedia.org/wiki/List_of_government...

    Department of Health Services; Department of Ayurveda and Alternative Medicine; Department of Forests and Soil Conservation; Department of National Parks and Wildlife Conservation; Department of Plant Resources; Department of Agriculture; Department of Livestock Services; Department of Food Technology and Quality Control; Department of Archaeology

  4. Nepal Bureau of Standards and Metrology - Wikipedia

    en.wikipedia.org/wiki/Nepal_Bureau_of_Standards...

    Nepal Bureau of Standards & Metrology (NBSM) is a department under the Ministry of Industry, Nepal. [1] The department was established in 1976 based on the Industrial policy (1974) with an aim to regulate and improve the quality of industrial production. The initial name of the department was Nepal Institute of Standards (NIS).

  5. Ministry of Industry, Commerce and Supplies - Wikipedia

    en.wikipedia.org/wiki/Ministry_of_Industry...

    The Nepal Institute of Standards was established in 1976, to develop national standards and to formulate concerning acts and rules. [13] In 1981, the Nepal Institute of Standards was renamed and restructured into the Nepal Bureau of Standards as a full-fledged department of the Ministry of Industry. [13]

  6. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    A stringent regulatory authority is a regulatory authority which is: a) a member of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), being the European Commission, the US Food and Drug Administration and the Ministry of Health, Labour and Welfare of Japan also represented by the Pharmaceuticals and Medical Devices Agency (as before ...

  7. Validation master plan - Wikipedia

    en.wikipedia.org/wiki/Validation_master_plan

    The GAMP 5 standard recommends an approach to the creation of the plan. [3]Topics commonly covered include: Introduction, scope, responsibilities, description of facility and design, building and plant Layout, cleanrooms and associated controlled environments, storage areas, personnel, personnel and material Flow, water and solid waste handling, infrastructure and utilities, water system ...

  8. Good documentation practice - Wikipedia

    en.wikipedia.org/wiki/Good_documentation_practice

    Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.

  9. GMP - Wikipedia

    en.wikipedia.org/wiki/GMP

    GMP may refer to: Finance and economics. Gross metropolitan product, a measure of goods and services produced; Guaranteed maximum price, as agreed in some contracts;