market authorization
1Market access — for goods in the WTO means the conditions, tariff and non tariff measures, agreed by members for the entry of specific goods into their markets. Tariff commitments for goods are set out in each member s schedules of concessions on goods. The… …
2Market — A place where goods may be bought or sold, established in a village or town with the authorization of a king or lord. This noble extends his protection to the market for a fee, and allows its merchants various economic and judicial privileges.… …
3Marketing authorization — Process of reviewing and assessing the dossier to support a medicinal product in view of its marketing (also called licensing, registration, approval, etc.), obviously finalized by granting of a document also called marketing authorization… …
4East New Market, Maryland — Infobox Settlement official name = East New Market, Maryland settlement type = Town nickname = motto = imagesize = image caption = image imagesize = image caption = image mapsize = 250x200px map caption = Location of East New Market, Maryland… …
5Options Market France — (OMF) is a futures exchange and clearing house. In November 1987 Options Market France started publishing in association with the French bank CCF now HSBC France a stock index using the Reuters network under the symbol EFX 50. The index was… …
6gray market goods — Foreign manufactured goods, bearing a valid United States trademark, that are imported without the consent of the U.S. trademark holder. The gray market arises in three general contexts. In the first case, despite a domestic firm s having… …
7gray market goods — Foreign manufactured goods, bearing a valid United States trademark, that are imported without the consent of the U.S. trademark holder. The gray market arises in three general contexts. In the first case, despite a domestic firm s having… …
8Marketing Authorization Application — is an application (to the relevant authority ; typically the UK s MHRA [1]or the European Commission s Committee for Medicinal Products for Human Use (CHMP)) to market a drug or medicine. The U.S. Food and Drug Administration equivalent is a …
9Supplementary protection certificate — In European Union member countries, a supplementary protection certificate (SPC) is a sui generis , patent like, intellectual property right. This type of right is available for medicinal products, such as drugs, and plant protection products,… …
10Novo Nordisk — A/S Type Publicly traded Aktieselskab (OMX: NOVO B, NYSE:  …
