Delegated and implementing regulations

This regulation lays down rules on appropriate measures to ensure the effective and safe use of veterinary medicinal products authorised and prescribed for oral administration via routes other than medicated feed and administered by the animal keeper to food-producing animals

This regulation concerns the requirements on compliance with good laboratory practice for veterinary medicinal products set out in Annex II.

This regulation establishes requirements for the collection of data on the volume of sales and on the use of antimicrobial medicinal products in animals (EN).

 This regulation is an amendment to the dossier requirements referred to in Annex II of Regulation (EU) 2019/6 (EN). (EN).

This regulation relates to the single lifetime identification document for equine animals (EN).

This regulation concerns the prohibition of use of certain antimicrobial medicinal products in animals or products of animal origin exported from third countries into the Union (EN).

This regulation (EU - 2025/2091) lays down good manufacturing practice for veterinary medicinal products.
 

This regulation (EU - 2025/2154) lays down good manufacturing practice for active substances used as starting materials in veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council.
 

This regulation (EU - 2025/901) establishes a list of substances which are essential for the treatment of equine species, or which bring added clinical benefit compared to other treatment options available for equine species and for which the withdrawal period for equine species shall be six months and repealing Regulation (EC) No 1950/2006.
 

This regulation amends Annex III to Implementing Regulation (EU) 2020/2235 and Annex II to Implementing Regulation (EU) 2021/403 as regards model certificates for the entry into the Union of consignments of certain products of animal origin and certain categories of animals

This regulation amends and corrects Annex III to Implementing Regulation (EU) 2020/2235 as regards model certificates for the entry into the Union of consignments of certain categories of animals and certain products of animal origin intended for human consumption, and correcting Implementing Regulation (EU) 2024/399

This regulation establishes a list of antimicrobials which shall not be used in accordance with Articles 112 and 113 of Regulation (EU) 2019/6 of the European Parliament and of the Council or which shall only be used in accordance with those Articles subject to certain conditions.

This regulation provides uniform rules on the size of small immediate packaging units of veterinary medicinal products, as erferred to in article 12 of REgulation (EU) 2019/6.

This regulation adopting a list of abbreviations and pictograms common throughout the Union to be used on the packaging of veterinary medicinal products for the purposes of Article 10(2) and Article 11(3) of Regulation (EU) 2019/6.

This regulation relates to the establishment of the format of the data to be collected and reported in order to determine the volume of sales and the use of antimicrobial medicinal products in animals (EN).

This regulation designates antimicrobials or groups of antimicrobials reserved for treatment of certain infections in humans (EN).

This regulation relates to the Union database on veterinary medicinal products (EN)

This regulation relates to the variations for which no assessment is required (EN).

This regulation relates to the identification and registration of equine animals and the establishment of model identification documents for those animals (EN).

This regulation relates to the measures on good distribution practice for active substances used as starting materials in veterinary medicinal products (GDP) (EN).

This regulation relates to good pharmacovigilance practice and the format, content and summary of the pharmacovigilance system master file for veterinary medicinal products (EN).

This regulation relates to measures on good distribution practice (GDP) for veterinary medicinal products (EN).

This regulation relates to the adoption of the design of a common logo for the retail of veterinary medicinal products at a distance (EN).