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Royal Philips
Company · Netherlands · EU Transparency Register 035366013790-68
Counts here are a floor, never a total: they cover the 326 consultation files tracked so far (29,503 submissions, mostly 2025–26), so an organization's real filing history is larger, not smaller.
Who they are
Among the 925 companies & groups on this site, they rank #82 by legislative files engaged — a count of participation, not a measure of influence.
Declares membership of
- AIM
- BusinessEurope →
- APPLiA
- Digital Europe →
- ERT
- COCIR →
- MedTech Europe →
- BDVA
- IP Europe →
- Friends of Europe
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026).
- Register category
- Companies & groups
- Registered as
- Koninklijke Philips (Philips)
- Head office
- Amsterdam, Netherlands
- EU office
- Brussels
Self-declared to the EU Transparency Register (snapshot 30 Aug 2026); cost bands are floors, not audited totals. Reused under Commission Decision 2011/833/EU.
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Their record over time
Royal Philips filed 7 positions between 7 Mar 2025 and 19 May 2026, across 7 of the 326 legislative files tracked here, attaching a full position paper 7 times.
What they argued
Many thanks for the opportunity to provide our feedback. You find here attached our recommendations for a revision of the Public Procurement Directive, as well as the overall framework for procurement of medical and digital health technologies in the European Union.
Thank you for the opportunity to comment on the targeted revision of the EU rules for medical devices. Philips shares the concerns as raised in the call for evidence. We believe a reform of the regulatory framework is necessary to ensure availability of medical devices for patients and to strenghten EU competitiveness. The announced revision is an important pilar of the EU Life Science Strategy.
Public procurement plays a critical role in addressing health systems' challenges through strategic purchasing decisions that focus on the value a given solution brings to the broader healthcare system. It can also be a powerful tool to drive innovation and the competitiveness of European industry.
We appreciate the efforts of the European Commission to simplify the taxonomy and welcome several of the proposed changes. However, we are still concerned that some of the criteria in this draft delegated act will exclude entire sub-sectors of electric and electronic equipment, including and especially manufacture of electro-medical equipment (medical devices), from alignment with the EU Taxonomy.
Thank you for the opportunity to contribute to the EU CVD Health Check Protocol. Philips strongly supports the European Commissions commitment to reducing premature mortality from cardiovascular diseases (CVD) across the EU by 2030. We recognize that the development and implementation of a comprehensive EU Protocol on Health Checks is a critical step toward achieving this ambitious and vital public health objective.
Duly responding to the increasing pressures of disasters and pandemics, the Union Civil Protection Mechanism and Union support for health emergency preparedness and response has as one of its objectives to increase supply of medical devices in the European Union, and fund procurement and stockpiling of medical countermeasures.
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Turns up on the same files
Organizations that also filed on at least two of the same consultations. A shared interest in the same dossiers — not evidence of coordination, and we do not suggest any.
- MedTech Europe · 7 files in common
- Siemens Healthineers · 6 files in common
- EFPIA · 5 files in common
- Cefic · 4 files in common
- Danish Chamber of Commerce · 4 files in common
Showing 5 of 320.
Is this your organization?
Everything on this page comes from Royal Philips’s own submissions to the European Commission — we have added nothing and interpreted nothing. If something is wrong or out of date, email info@policyspeak.com and we will correct it. If you are an individual named in a record, our privacy policy sets out your rights to correction, objection and removal.
Quotes are verbatim from submissions published by the European Commission, trimmed to their opening passage and never summarized by a model. Organizations only, never individuals. Reused under Commission Decision 2011/833/EU; the European Commission is not liable for this reuse.