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.
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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  • Medicinal products that were suspended or withdrawn, or for which a marketing authorisation was refused.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.