The European Medicines Agency (EMA) website presents information on regulatory topics in the three main stages of the medicinal product lifecycle, to help users find information as easily as possible.
The navigation menu contains three main sections corresponding to the key medicinal product lifecycle stages:
- research and development, including maximum residue limits (MRLs);
- marketing authorisation;
Each main section provides an overview on a landing page, with sub-topics in the sub-menu in alphabetical order.
Some regulatory topics span the product lifecyle. Entry pages on these transversal topics are in this overview section, in the sub-menu in alphabetical order: