View source for Medicine:Marketing Authorization Application

'''Marketing Authorisation Application''' ('''MAA''') is an application submitted by a drug manufacturer seeking permission to bring a medicinal product (for example, a new medicine or generic medicine) to the market.
MAA is part of the official procedure before the [[Organization:Medicines and Healthcare products Regulatory Agency|Medicines and Healthcare products Regulatory Agency]] in the {{wipe|United Kingdom}}<ref>{{cite web|url=http://www.mhra.gov.uk/Howweregulate/Medicines/Licensingofmedicines/Marketingauthorisations/index.htm|title=Apply for a licence to market a medicine in the UK - GOV.UK|website=www.mhra.gov.uk}}</ref> and the Committee for Medicinal Products for Human Use of the European Commission. In the {{wipe|United States}}, the equivalent process is called [[Chemistry:New Drug Application|New Drug Application]].

==See also==
* [[Organization:European Medicines Agency|European Medicines Agency]]
* [[Medicine:Identification of medicinal products|Identification of medicinal products]]
==References==
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[[Category:Drug safety]]

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