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Home > Knowledge > Health and Medical Service
GMP for Pharmaceuticals

GMP
(note: GMP is the abbreviation of Good Manufacturing Practice)

  1. Explanation:

    The manufacturers of pharmaceutical products applying for registration of factory establishment, or for altering registration of factory for manufacturing new drugs, should conform to the regulation of Good Manufacturing Practice (GMP) and submit relevant materials when making application. Such materials should be presented to the bureaus of consruction under provincial or municipal governments, and afterwards be transferred to Industrial Development Bureau, Ministry of Economic Affairs, and Department of Health, Executive Yuan for approval.
    GMP pharmaceutical factories can be divided into western pharmaceutical factories manufacturing western pharmaceutical products, traditional pharmaceutical factories manufacturing traditional pharmaceutical products in the type of western pharmceutical doses, and traditional pharmaceutical factories manufacturing traditional pharmaceutical products in the type of Chinese medicine (such as wan, san, etc.)
    　
  2. Sponsoring Agency:

    Department of Health, Executive Yuan, and Ministry of Economic Affairs, Executive Yuan.

    Department of Health, Executive Yuan

    Address (Zip code): (100) No.100, Aikuo East Road, Chungchen, Taipei
    Website:http://www.doh.gov.tw/
    Telephone:(02)2321-0151 extend to Bureau of Pharmaceutical Affairs
    (02)2393-3119 extend to Committee on Chinese Medicine and Pharmacy
    Fax:(02)2397-1548(02)2391-4897
    Website: http://www.ccmp.gov.tw/
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