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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 ...
The Drug Regulatory Authority of Pakistan was established in 2012 and is the largest department in the Ministry of National Health Services, Regulation and Coordination, with its headquarters in Islamabad and regional offices in the provincial capitals of Karachi, Lahore, Peshawar and Quetta. DRAP has been established by the Federal Government ...
It is similar in function to the Food and Drug Administration in the United States, the Medicines and Healthcare products Regulatory Agency in the United Kingdom, the Spanish Agency of Medicines and Medical Devices in Spain or the Food and Drug Administration in the Philippines. [2] The PhMDA has been eCTD compliant at least since December 2017 ...
25 Ministry of National Health Services, Regulation and Coordination 26 Ministry of Overseas Pakistanis and Human Resource Development 27 Ministry of Parliamentary Affairs
It was discovered that 95.6% (324 firms) were violating the Labor Standards Law and the Industrial Safety and Health Law. 219 businesses (64.6%) broke the law by having their drivers work behind the wheel more than the legal maximum of eight hours a day and 40 hours a week, or longer than what was agreed upon with their labour union. It also ...
Sakigake (さきがけ, lit. "pathfinder", "harbinger") is a drug designation by the Pharmaceuticals and Medical Devices Agency, the pharmaceuticals regulator of Japan.It was designed to provide easier access to novel advanced treatments. [1]
Pakistan Medical and Dental Council is a statutory regulatory authority that maintains the official register of medical practitioners in Pakistan. Its chief function is to establish uniform minimum standards of basic and higher qualifications in medicine and dentistry throughout Pakistan.
The Global Harmonization Task Force (GHTF) was “a voluntary group of representatives from national medical device regulatory authorities (such as the U.S. Food and Drug Administration (FDA)) and the members of the medical device industry” [1] whose goal was the standardization of medical device regulation across the world.