The Union Register lists all medicinal products for human and veterinary use as well as orphan medicinal products that have received a marketing authorisation by the Commission through the centralised procedure. Medicinal products that have received a marketing authorisation by Member States are not listed in the Union Register.
What inside?
- Medicinal products on the EU market
- Medicinal products that were suspended or withdrawn, or for which a marketing authorisation was refused.
- Medicinal products for human and veterinary use adopted nationally for which a Commission decision was necessary.
- Commission decisions adopted in the last six months.
- Medicinal products authorised by individual EU countries under Article 126a of Directive 2001/83.
- A general index of active substances covered by Commission decisions.
- A general index of medicinal products listed by the brand name covered by Commission decisions.
