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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 ...
Food and Drug Administration (Thai FDA) 2016 Turkey: Turkish Medicines and Medical Devices Agency (TMMDA) 2018 Ukraine: State Service for Medications and Drugs Control (SMDC) 2011 United Kingdom: Medicines and Healthcare products Regulatory Agency (MHRA) Veterinary Medicines Directorate (VMD) 1999 2014 United States: U.S. Food and Drug ...
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The Act authorizes several subsidiary organizations, including the Bhutanese Drug Regulatory Authority, Drug Testing Laboratory, and teams of Drug Inspectors. These agencies have rulemaking and law enforcement authority on drugs, medicines, and even price controls, but must operate within the laws of Bhutan. [14]
The Ministry of Health was one of the first 13 Ministries of the Provisional Revolutionary Government of the Democratic Republic of Vietnam, [2] [3] [4] established on August 28, 1945 [5] and introduced to the people for the first time on September 2, 1945. The first Minister was Doctor Pham Ngoc Thach.
The Government of the Socialist Republic of Vietnam (Vietnamese: Chính phủ nước Cộng hòa xã hội chủ nghĩa Việt Nam; less formally the Vietnamese Government or the Government of Vietnam, Vietnamese: Chính phủ Việt Nam) is the cabinet and the central executive body of the state administration of Vietnam.
Regulatory Authority for Audiovisual and Digital Communication Autorité de la Concurrence French Polynesia: Service des Postes et Télécommunications de Polynésie Française Gabon: Autorité de Régulation des Communications Électroniques et des Postes Gambia: Gambian Public Utilities Regulatory Authority Georgia
The health bureaucrats pursued this agenda again in October, at the International Conference of Drug Regulatory Authorities (ICDRA), and again in December 2012 at the Heads of Medicines Regulatory Agencies Summit. "As a result, a consensus has emerged on the desirability of developing an ICMRA to address common issues." [3]