Packaging and labelling of veterinary medicinal products: transitional rules
Laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised in accordance with Directive 2001/82/EC and Regulation (EC) No 726/2004
- Stage
- In force, reached 31 May 2022
- In force
- In force since 28 Jan 2022 · CELEX 32022R0839
- Procedure
- Ordinary legislative procedure
- Last activity
- 8 Jun 2022
Where it stands
Latest: Discussions within the Council or its preparatory bodies, 8 Jun 2022.
ShowHide the earlier record: 7 dates, 2 Mar 2022 to 5 May 2022
- 2 Mar 2022
- Adoption by Commission
- 4 Mar 2022
- Discussions within the Council or its preparatory bodies
- 7 Mar 2022
- Plenary sitting
- Referred to committee
- 28 Apr 2022
- Discussions within the Council or its preparatory bodies
- Feedback on adopted proposal closed: Transitional regime for packaging and labelling of veterinary medicinal products, 1 responses · Commission
- 2 May 2022
- Plenary sitting
- 3 May 2022
- Plenary vote
- 5 May 2022
- Discussions within the Council or its preparatory bodies
- EP position at first reading
- Plenary amended the proposal
- Plenary vote
- 6 May 2022
- Discussions within the Council or its preparatory bodies
- 16 May 2022
- Approval of the EP's first reading position by the Council (adoption of the legislative act)
- 18 May 2022
- Plenary sitting
- 19 May 2022
- Discussions within the Council or its preparatory bodies
- 30 May 2022
- Signed
- 31 May 2022
- Published in the Official Journal
- 6 Jun 2022
- Plenary sitting
- 8 Jun 2022
- Discussions within the Council or its preparatory bodies
Documents
Newest first. Each opens at its source.
- Text adopted · OJ L 148 31.05.2022, p. 0006Commission
- Text adopted · Regulation 2022/0839Commission
- Text adopted · SP(2022)324Parliament
- Text adopted · T9-0198/2022Parliament
Consultations on it
The Commission's Have Your Say consultations linked to this file. Each title opens on the Commission's portal.
| Consultation | Feedback deadline | Feedback received |
|---|---|---|
| 28 Apr 2022 | 1 |
Summary
GeneratedThis regulation establishes transitional rules for packaging and labelling of veterinary medicinal products authorized under Directive 2001/82/EC and Regulation (EC) No 726/2004. It allows existing products to remain on the market without immediate redesign to comply with new EU rules, affecting pharmaceutical manufacturers, distributors, and veterinarians.
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A first draft
Sources: EP Legislative Observatory · EUR-Lex. Record as of 14 Sept 2026. Something wrong on this page? Report an error.
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