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Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)

Chapter IV POST-MARKETING AUTHORISATION MEASURES

United Kingdom

Original text. Later amendments are not shown.

1Union product database
2Collection of data by Member States and responsibilities of marketing authorisation holders
3Changes to the terms of the marketing authorisations
4Harmonisation of the summaries of product characteristics for nationally authorised products
5Pharmacovigilance
6Union interest referral

Chapter IV

Legislation: Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)
Citation: EU Regulation 2019/6, chapter iv
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright