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.
RM
Revitalised Medicine
NGO · United States
not in the EU Transparency RegisterThis organization files on consultations without a register number, so its record here is built from its filings alone. Register facts (staff, costs, accreditations) are not available for it.
3
positions filed
in the 665 files tracked
3
legislative files
of 665 tracked
0
with a full position paper
attached to a submission
Counts here are a floor, never a total: they cover the 665 consultation files tracked so far (57,774 submissions, mostly 2021–26), 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 665 legislative files tracked here.
What they argued
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).
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.
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