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Regulation (EU) 2022/8392022/0053(COD)COM(2022)76

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
20 entries · record as of 14 Sept 2026

Where it stands

Latest: Discussions within the Council or its preparatory bodies, 8 Jun 2022.

Show the earlier record: 7 dates, 2 Mar 2022 to 5 May 2022
  1. 2 Mar 2022
    • Adoption by Commission
  2. 4 Mar 2022
    • Discussions within the Council or its preparatory bodies
  3. 7 Mar 2022
    • Plenary sitting
    • Referred to committee
  4. 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
  5. 2 May 2022
    • Plenary sitting
  6. 3 May 2022
    • Plenary vote
  7. 5 May 2022
    • Discussions within the Council or its preparatory bodies
    • EP position at first reading
    • Plenary amended the proposal
    • Plenary vote
  1. 6 May 2022
    • Discussions within the Council or its preparatory bodies
  2. 16 May 2022
    • Approval of the EP's first reading position by the Council (adoption of the legislative act)
  3. 18 May 2022
    • Plenary sitting
  4. 19 May 2022
    • Discussions within the Council or its preparatory bodies
  5. 30 May 2022
    • Signed
  6. 31 May 2022
    • Published in the Official Journal
  7. 6 Jun 2022
    • Plenary sitting
  8. 8 Jun 2022
    • Discussions within the Council or its preparatory bodies
4 documents

Documents

Newest first. Each opens at its source.

1 consultation

Consultations on it

The Commission's Have Your Say consultations linked to this file. Each title opens on the Commission's portal.

ConsultationFeedback deadlineFeedback received
28 Apr 20221

Summary

Generated

This 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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Sources: EP Legislative Observatory · EUR-Lex. Record as of 14 Sept 2026. Something wrong on this page? Report an error.

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