Marketing Authorisation Application


Marketing Authorisation Application is an application submitted by a drug manufacturer seeking marketing authorisation, that is permission to bring a medicinal product to the market.
MAA is part of the official procedure before the Medicines and Healthcare products Regulatory Agency in the United Kingdom and the Committee for Medicinal Products for Human Use of the European Medicines Agency, a specialised agency of the European Commission. In the United States, the equivalent process is called New Drug Application.