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Dossier · Resolution on a topical subject

Urgent need to revise the medical devices regulation

Reference
2024/2849(RSP) Resolution on a topical subject
Where it stands
Parliament adopted the text on 23 October 2024. This is its final position on the matter.
Stage
Parliament’s position
More facts (3)
Decisions in plenary
1
Versions
10 versions

Where it stands

The steps of this kind of dossier and how far it has come, from the procedure file.

  1. Tabled for plenary (done)
  2. Plenary vote (done) Adopted 23 October 2024
  3. Parliament’s position (done) Final

A resolution tabled by political groups, usually on an urgent matter or in reaction to a statement by the Commission or Council. Not binding.

People

Committees and members responsible for the dossier, as the procedure file names them. Groups as recorded there.

The procedure file names no committee or rapporteur for this dossier.

Decisions in plenary, 1

Every decision Parliament took on this dossier, newest first.

Effect: what the decision did. Final vote: for–against–abstained, and how it was recorded.
DateDecisionKindEffectFinal vote
23 Oct 2024Urgent need to revise the Medical Devices Regulation ResolutionsAdoptedshow of hands — no count

Voting grid

Export

Every roll-call vote on the dossier, in date and voting order, with each group's line at the date of the vote.

Each group's clear line at the date of the vote: a position with at least two thirds of the group's votes (at least 10 members voting), otherwise Divided; “< 10 voted” when fewer took part. Result: outcome, for–against–abstained (method).

  1. Adopted 545–80–15

    The Left
    Against
    Greens
    For
    S&D
    For
    Renew
    For
    EPP
    For
    ECR
    For
    Patriots
    Divided
    ESN
    For
  2. Adopted 420–208–12

    The Left
    Against
    Greens
    For
    S&D
    Against
    Renew
    For
    EPP
    For
    ECR
    For
    Patriots
    Divided
    ESN
    For

Versions, 10

The text of the dossier, version by version, newest first. Compare shows what changed between two consecutive versions.

  1. Adopted by Parliament23 Oct 2024

    Adopted text TA10-0028/2024 TA-10-2024-0028

    Compare with tabled for plenary

  2. Tabled for plenary21 Oct 2024

    Joint motion RC-B10-0123/2024 RC-10-2024-0123

    Compare with tabled for plenary

  3. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0125/2024 B-10-2024-0125

  4. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0124/2024 B-10-2024-0124

  5. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0121/2024 B-10-2024-0121

  6. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0126/2024 B-10-2024-0126

  7. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0122/2024 B-10-2024-0122

  8. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0127/2024 B-10-2024-0127

  9. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0123/2024 B-10-2024-0123

  10. Tabled for plenary16 Oct 2024

    Motion for a resolution B10-0128/2024 B-10-2024-0128

AI: Each version in short Written by AI from the official text — check the source
  • Adopted text TA10-0028/2024: Parliament calls on the Commission to propose delegated and implementing acts by the end of Q1 2025 and a systematic revision of the Medical Devices Regulation and the In Vitro Diagnostic Medical Devices Regulation, with an impact assessment, to address implementation challenges.
  • Motion for a resolution B10-0125/2024: This resolution calls on the Commission to propose a systematic revision of the Medical Devices Regulation and the In Vitro Diagnostic Medical Devices Regulation within the first hundred days of the new mandate.
  • Motion for a resolution B10-0124/2024: This resolution addresses the urgent need to revise the Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR), citing shortages, access inequalities, and administrative burdens.
  • Motion for a resolution B10-0121/2024: This resolution addresses the urgent need to revise the Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR), expressing support for strict patient safety and calling for improved implementation and transparency.
  • Motion for a resolution B10-0126/2024: Parliament stresses support for swift implementation of the Medical Devices Regulation and In Vitro Medical Devices Regulation, and urges action to prevent device shortages, improve transparency, and strengthen post-market surveillance.
  • Motion for a resolution B10-0122/2024: The resolution calls for urgent revision of the Medical Devices Regulation and the In Vitro Diagnostic Medical Devices Regulation, citing excessive bureaucracy, certification backlogs, and product shortages.
  • Motion for a resolution B10-0127/2024: Parliament calls on the Commission to propose a revision of the Medical Devices Regulation and the In Vitro Diagnostic Medical Devices Regulation to address implementation challenges.
  • Motion for a resolution B10-0123/2024: This resolution addresses the urgent need to revise the Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). It calls for action to improve implementation, harmonise procedures, and ensure patient safety.
  • Motion for a resolution B10-0128/2024: Parliament expresses concern about delays in implementing the Medical Devices Regulation (MDR) and calls on the Commission to urgently revise it to simplify approval procedures, reduce administrative burden, and address unmet medical needs.

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What changed, 1

Between consecutive versions, newest pair first. The overviews are written by AI from the two texts; the comparison shows every change.

  1. Latest Tabled for plenary → Adopted by Parliament Joint motion RC-B10-0123/2024 → Adopted text TA10-0028/2024

    AI: What changed Written by AI from the official text — check the source

    The new version adds two recitals and one paragraph on substance-based medical devices and e-health applications, calling for their inclusion in the revised regulation to protect health data and foster innovation.

    Read the changes · Report a problem

    Compare the two versions

Timeline, 2

Every recorded step, newest first, grouped by stage; the latest stage is open.

Connections

Texts, decisions, people and other dossiers related to this one.

Sources & citation

Where the facts on this page come from, and how to cite it.

Data source
Licensed CC BY 4.0.
Retrieved
25 September 2026

Cite as

European Parliament (2024). “Urgent need to revise the medical devices regulation”. Dossier, 23 October 2024. procId 2024-2849, reference 2024/2849(RSP). EU Parl Watch Research. https://news.eu-parl.st-solutions.dev/dossiers/2024-2849 (retrieved 25 September 2026). Official source: Procedure file (Legislative Observatory, OEIL), https://oeil.secure.europarl.europa.eu/oeil/en/procedure-file?reference=2024%2F2849(RSP). Data: EP Open Data API: procedure record, https://data.europarl.europa.eu/api/v2/procedures/2024-2849 (CC BY 4.0).
BibTeX
@misc{epw-dossier-2024-2849,
  author = {{European Parliament}},
  title = {{Urgent need to revise the medical devices regulation}},
  year = {2024},
  date = {2024-10-23},
  howpublished = {\url{https://news.eu-parl.st-solutions.dev/dossiers/2024-2849}},
  url = {https://news.eu-parl.st-solutions.dev/dossiers/2024-2849},
  urldate = {2026-09-25},
  publisher = {EU Parl Watch Research},
  note = {Dossier. procId 2024-2849, reference 2024/2849(RSP). Official source: https://oeil.secure.europarl.europa.eu/oeil/en/procedure-file?reference=2024\%2F2849(RSP). Data: EP Open Data API: procedure record (CC BY 4.0)}
}