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2. Regulatory affairs - Wikipedia

   en.wikipedia.org/wiki/Regulatory_affairs

   Regulatory affairs (RA), is a profession that deals with an organization’s adherence to regulatory compliance.. It is a position mostly found within regulated industries, such as pharmaceuticals, medical devices, cosmetics, agrochemicals (plant protection products and fertilizers), energy, banking, telecom etc. Regulatory affairs also has a very specific meaning within the healthcare ...

3. 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 ...

4. Academy of Applied Pharmaceutical Sciences - Wikipedia

   en.wikipedia.org/wiki/Academy_of_Applied...

   2004: AAPS becomes the first private career college to offer a diploma program in Professional Regulatory Affairs. 2005: AAPS launched the Continuing Education unit, providing workshop, courses, and certificate training for pharmaceutical industry careers.

5. Pharmaceutical physician - Wikipedia

   en.wikipedia.org/wiki/Pharmaceutical_physician

   Training in pharmaceutical medicine usually involves a blend of on-the-job experience and formal education, such as obtaining the Diploma in Pharmaceutical Medicine. Over a four-year training period, pharmaceutical physicians acquire expertise in various areas, including regulatory affairs, pharmacology, drug safety, clinical development, and ...

6. Medicines and Healthcare products Regulatory Agency

   en.wikipedia.org/wiki/Medicines_and_Healthcare...

   The MHRA and the US Food and Drug Administration were criticised in the 2012 book Bad Pharma, [43] and in 2004 by David Healy in evidence to the House of Commons Health Committee, [44] for having undergone regulatory capture, i.e. advancing the interests of the drug companies rather than the interests of the public.

7. Office of Global Regulatory Operations and Policy - Wikipedia

   en.wikipedia.org/wiki/Office_of_Global...

   FDA Building 32 houses the Office of the Commissioner and the Office of Regulatory Affairs. The Office of Global Regulatory Operations and Policy (GO), [1] also known as the Office of Regulatory Affairs (ORA), [2] is the part of the U.S. Food and Drug Administration (FDA) enforcing the federal laws governing biologics, cosmetics, dietary supplements, drugs, food, medical devices, radiation ...