37 organisations appear across 94 disclosed European Commission meetings on healthcare & medical devices; the top listed organisations are MedTech Europe, European Coordination Committee of the Radiological, Electromedical and healthcare IT Industry, European Patients' Forum (EPF). Source: European Commission meeting disclosures and the EU Transparency Register. Methodology
Who lobbies the EU on Healthcare & Medical Devices?
Healthcare, medtech and digital-health companies face EU rules on medical devices, diagnostics and health data. These are the EU acts most likely to apply.
Ranked by distinct disclosed European Commission meetings whose topic matches healthcare & medical devices keywords. 37 organisations appear across 94 such meetings. Every organisation links to the official disclosure.
- 1MedTech Europe20 mtgse.g. Medical devices reformsource ↗
- 2European Coordination Committee of the Radiological, Electromedical and healthcare IT Industry13 mtgse.g. Exchange on matters related to the interplay between the medical devices regulations and the AI Act and on the upcoming conference on medical devices.source ↗
- 3e.g. Discussion of the EPF's current activities and planned actions with respect to the implementation of the Health Technology Assessment Regulation (HTAR).source ↗
- 4e.g. Exchange of views on the current state of play of the medical devices Regulations reform proposal and discussion on the organisation of a conference on medical devices on the 16th of March 2026.source ↗
- 5e.g. Exchange of views on the state of play and next steps for the medical devices sectorsource ↗
- 6e.g. Medical device reviewsource ↗
- 7Siemens Healthineers AG3 mtgse.g. Challenges faced by the medical devices industrysource ↗
- 8
- 9Carl Zeiss AG2 mtgse.g. Medical device reviewsource ↗
- 10MedicalMountains GmbH2 mtgse.g. Medical device reviewsource ↗
- 11Koninklijke Philips2 mtgse.g. Challenges faced by the medical devices industrysource ↗
- 12e.g. Challenges faced by the medical devices industrysource ↗
- 13
- 14e.g. Exchange of views on the state of play and next steps for the medical devices sector.source ↗
- 15e.g. Exchange of views on the state of play and next steps for the medical devices sector.source ↗
- 16e.g. Exchange of views on the state of play and next steps for the medical devices sectorsource ↗
- 17e.g. Exchange on matters related to the MDCG CIEPSE WG and on the upcoming conference on medical devicessource ↗
- 18e.g. Exchange of views on the state of play and next steps for the medical devices sector.source ↗
- 19e.g. Medical device reviewsource ↗
- 20e.g. Life science strategy and medical device technologiessource ↗
- 21e.g. European medical device industry in Chinasource ↗
- 22Edwards Lifesciences1 mtge.g. Discussion on the importance of innovation in the medical devices sectorsource ↗
- 23Greiner AG1 mtge.g. Ongoing activities of the two subgroups of the Technology Council Industrial uptake of advanced materials innovation R&I needs for medical devicessource ↗
- 24e.g. Exchange of views on novel medical devicessource ↗
- 25
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Frequently asked
Who lobbies the EU on healthcare & medical devices?
Based on disclosed European Commission meetings, the most active organisations include MedTech Europe, European Coordination Committee of the Radiological, Electromedical and healthcare IT Industry, European Patients' Forum (EPF), Biomedical Alliance in Europe, Confindustria Dispositivi Medici. 37 organisations appear across 94 disclosed meetings on these topics.
How is "Healthcare & Medical Devices" lobbying measured here?
By counting distinct, officially disclosed Commission meetings whose topic matches healthcare & medical devices keywords (medical device, in vitro diagnostic, European Health Data Space, health technology assessment). These are disclosed meetings, not a measure of influence, and each is linked to its official source.
Primary sources
Rankings count distinct disclosed Commission meetings whose topic matches the sector keywords; they are not a measure of influence. Methodology. Data © European Union (Decision 2011/833/EU).
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