The Union Register is the European Commission's official register for medicinal products authorised through the EU centralised procedure.
Official resources
What it provides
Records can be searched by product name, active substance or EU registration number and include authorisation details such as the marketing-authorisation holder, active substance, ATC code, therapeutic indication and associated regulatory documents.
The Register also includes information on products that have been suspended, withdrawn or refused.
Practical use
Use the Union Register when the legally relevant Commission authorisation record is needed, particularly for centralised products and implementation of Commission decisions. It complements EMA's EPAR pages: EMA provides the scientific and procedural record, while the Commission register provides the formal authorisation record.