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Regulation (EU) 2021/2282 of the European Parliament and of the Council of 15 December 2021 on health technology assessment and amending Directive 2011/24/EU (Text with EEA relevance) article 20 CELEX: 32021R2282 Adoption of detailed procedural rules for joint scientific consultations
1. After consulting the Coordination Group, the Commission shall adopt, by means of implementing acts, detailed procedural rules for: (a) submission of requests from health technology developers; (b) the selection and consultation of stakeholder organisations and patients, clinical experts and other relevant experts in joint scientific consultation; (c) cooperation, in particular by exchange of information, with the European Medicines Agency on joint scientific consultations on medicinal products where a health technology developer requests the consultation to be carried out in parallel with a process for scientific advice from the European Medicines Agency; (d) cooperation, in particular by exchange of information, with the expert panels on the joint scientific consultations on medical devices where a health technology developer requests the consultation to be carried out in parallel with the consultation of those expert panels. 2. Implementing acts referred to in paragraph 1 of this Article shall be adopted in accordance with the examination procedure referred to in Article 33(2). |