Article summary
The European Commission has launched a consultation on a draft implementing act on joint scientific consultations on medical devices and in vitro medical devices under Regulation (EU) 2021/2282 (the Health Technology Assessment (HTA) Regulation). The consultation covers the procedural rules of the draft act including, the submission of requests from health technology developers, the selection and consultation of stakeholders and experts, and co-operation with independent experts who support the scientific assessments and advice. The deadline for submitting responses is 26 November 2024.
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