- Draft published for feedback until 15 December 2023 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2024/875 adopted on 21 March 2024
- Draft published for feedback until 15 December 2023 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2024/878 adopted on 21 March 2024
- 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
- Commission Implementing Regulation (EU) 2023/997 (amending Commission Implementing Regulation (EU) 2021/17) adopted on 23 May 2023
- Commission Implementing Regulation (EU) 2024/916 (amending Commission Implementing Regulation (EU) 2021/17) adopted on 26 March 2024
- Commission Implementing Regulation (EU) 2025/163 amending Commission Implementing Regulation (EU) 2021/17 adopted on 30 January 2025
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 8 June 2021 (midnight Brussels time)
- AHE Feedback
- Commission Implementing Regulation (EU) 2021/1281 adopted on 2 August 2021
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted Stakeholder Consultation
- Draft published for feedback until 8 June 2021 (midnight Brussels time)
- AHE Feedback
- Commission Implementing Regulation (EU) 2021/1281 adopted on 2 August 2021
- Mandate from Commission to EMA
- EMA advice to EC
- Targetted stakeholder Consultation
- Draft on good manufacturing practice for active substances used as starting materials published for feedback until 19 February 2025 (midnight Brussels time)
- Draft on good manufacturing practice for veterinary medicinal products published for feedback until 19 February 2025 (midnight Brussels time)
- 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
- Mandate from Commission to EMA
- EMA advice to EC
- Draft published for feedback until 20 June 2024 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2024/1973 of 18 July 2024
- Mandate from the Commission to EMA regarding equines’
- Draft published for feedback until 04 March 2021 (midnight Brussels time)
- Commission Implementing Regulation (EU) 2021/963 adopted on 10 June 2021
- Mandate from Commission to EMA
- EMA advice to EC
- Addendum to EMA advice
- Background to the addendum
- Draft published for feedback until 12 February 2025 (midnight Brussels time)