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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 ...
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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.
Bhutan: Royal Monetary Authority of Bhutan: Bolivia: Autoridad de Supervisión del Sistema Financiero (ASFI) Bosnia and Herzegovina: Central Bank of Bosnia and Herzegovina ; Securities Commission of the Federation of Bosnia and Herzegovina (KOMVP) Botswana: Bank of Botswana ; Non-Bank Financial Institutions Regulatory Authority (NBFIRA) Brazil
The European Union (EU) medicines regulatory system is based on a network of around 50 regulatory authorities from the 31 EEA countries (28 EU Member States plus Iceland, Liechtenstein and Norway), the European Commission and European Medicines Agency (EMA). EMA and the Member States cooperate and share expertise in the assessment of new ...
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.
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]