Q&A

Navigating The MA Process When Launching A Drug Product In Europe

Source: Almac Group
Navigating The MA Process When Launching A Drug Product In Europe

To be able to market a medicinal product in Europe, you must obtain a Marketing Authorization (MA) from the relevant regulatory authority. There are a number of different routes to apply for an MA depending on the markets you wish to launch your drug product onto. It is worth considering long term goals as well as immediate plans at this stage.

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