| posp. |
заявление на выдачу регистрационного удостоверения (Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking permission to bring a newly developed medicinal product (for example, a new medicine) 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 Commission. In the United States, the equivalent process is called New Drug Application. WK Alexander Demidov) |
gov.ua kurzova); заявление о государственной регистрации лекарственного препарата (Rada0414)