Direct links to COVID-19 related medicinal products
Vaccines
Treatments
Direct links to Monkeypox related medicinal products
Vaccines
Treatments
NEW :
- As part of the Commission Pharmaceutical Strategy for Europe and EU Open Data initiative, datasets representing the information available on the Union Register will be regularly published here (and on the European Data portal once this project leaves the BETA stage).
- Available datasets:
- Licence: Creative Commons Attribution 4.0 International
- This service is currently in BETA stage. Feel free to provide your comments / feedback by clicking on this button:
Procedures for centrally authorised medicinal products1
Union Register of medicinal products for human use2
| Active | By EU number | Alphabetical |
| Withdrawn, suspended, expired, not renewed or revoked | By EU number | Alphabetical |
| Refused | Alphabetical |
Community Register of orphan medicinal products for human use3
| Active | By EU number | Alphabetical |
| Withdrawn or expired | By EU number | Alphabetical |
| Refused | Alphabetical |
Union Register of veterinary medicinal products4
| Active | By EU number | Alphabetical |
| Withdrawn, suspended, expired, not renewed or revoked | By EU number | Alphabetical |
| Refused | Alphabetical |
Procedures for nationally authorised medicinal products
Other links
IMPORTANT :
- Please note that the original, signed paper version of the Commission decision and associated annexes will not be sent to marketing authorisation holders by courier. It will be only sent by e-mail with a request to acknowledge receipt of the documents.
- Please ensure that someone is available to access the contact e-mail address you have supplied to the European Medicines Agency and to send an acknowledgement of receipt of the documents. Please check e-mails regularly if you are expecting to receive a Commission decision.
1 Variation procedures which do not affect the Commission Decision granting the marketing authorisation (including its annexes) are no longer reflected in the Union Register of medicinal products since 1 April 2011.
2 The Register of medicinal products for human use authorised by the EU under the centralised procedure. Published in accordance with Article 13 of Regulation (EC) No 726/2004.
3 The Register of orphan medicinal products for human use designated and published by the EU in accordance with Article 5 of Regulation (EC) No 141/2000.
4 The Register of veterinary medicinal products authorised by the EU under the centralised procedure. Published in accordance with Article 38 of Regulation (EC) No 726/2004.
5 The list of Exceptional Marketing Authorisations is published in accordance with Article 126a of Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the community code relating to medicinal products for human use.