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RM

Revitalised Medicine

NGO · United States

3
positions filed
in the 326 files tracked
3
legislative files
of 326 tracked
0
with a full position paper
attached to a submission

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.

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Their record over time

Revitalised Medicine filed 3 positions between 2 Jan 2026 and 7 Mar 2026, across 3 of the 326 legislative files tracked here.

What they argued

Simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and support of the European Medicines Agency for the expert panels on medical devices and the list of Union harmonisation legislationfiled 7 Mar 2026source

Revitalised Medicine supports the Commission for its development of expert panels and regulation that promotes specialised, advanced, and ethical medical device use through the revision of rules regarding medical devices and in vitro diagnostics.

European Biotech Actfiled 3 Mar 2026source

Revitalised Medicine praises the Commission for making significant improvements in the way innovation is pursued through the Biotech Act, and this regulation proposal addresses many issues in institutional frameworks (e.g. regarding personnel, data sharing, and technological integration).

European Health Data Space Board operationsfiled 2 Jan 2026source

As a U.S-based biohealth stakeholder that has previously collaborated with other stakeholders on EU public health policy, Revitalised Medicine welcomes this ideas on strengthening the European Health Data Space (EHDS) through collaborations with public service institutions and advocating for interactions between the EHDS board and the eHealth Network.

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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.

Showing 5 of 47.

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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.