# 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), Article 96: Record keeping

Extent: E+W+S+N.I.

1. The holder of a manufacturing authorisation shall record the following information in respect of all veterinary medicinal products that it supplies:
(a) date of the transaction;
(b) name of the veterinary medicinal product, and marketing authorisation number if applicable, as well as pharmaceutical form and strength, as appropriate;
(c) quantity supplied;
(d) name or company name and permanent address or registered place of business of the recipient;
(e) batch number;
(f) date of expiry.
2. The records referred to in paragraph 1 shall be available for inspection by competent authorities for one year after the date of expiry of the batch or at least five years from recording, whichever is longer.

---
Source: https://www.legislation.gov.uk/eur/2019/6/article/96 (the official version)
Page: https://openlegislation.uk/eu-regulation-2019-6/article-96
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.