- Mandate from Commission to EMA
- EMA advice to EC
- Amended EMA advice to EC
- Draft published for feedback until 17 May 2022 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2022/1255, adopted on 19 July 2022
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 07 August 2020 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/16 adopted on 8 January 2021
Format for the collection of data on antimicrobial medicinal products used in animals (Article 57 (4))
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 21 December 2021 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2022/209 adopted on 16 February 2022
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 07 August 2020 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/17 adopted on 8 January 2021
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 9 June 2021 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/1280 adopted on 2 August 2021
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 9 June 2021 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/1248 adopted on 29 July 2021
- Targetted Stakeholder Consultation
- Draft published for feedback until 07 August 2020 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/1904 adopted on 29 October 2021
- Draft published for feedback until 04 March 2021 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/963 adopted on 10 June 2021
- Uniform rules on the identification code for the packaging of a veterinary medicinal product (Article 17 (1))
- List of the abbreviations and pictograms common throughout the Union to be used in the packaging of a veterinary medicinal products (Article 17 (2))
- Rules on the size of small immediate packaging units (Article 17 (3))
- Functioning of the work-sharing procedure for variations (Article 65 (4))
- Model format for veterinary prescriptions (Article 105 (8))
- List of substances used in veterinary medicinal products authorised in the Union for use in food-producing terrestrial animal species or substances contained in a medicinal product for human use authorised in the Union which may be used in food-producing aquatic species (Article 114 (3))