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Commission Implementing Regulation (EU) 2025/2086 of 17 October 2025 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medical devices and in vitro diagnostic medical devices at Union level, as well as templates for those joint clinical assessments

Regulation

EUV 2025/2086:2025-10-17

Commission Implementing Regulation (EU) 2025/2086 of 17 October 2025 laying down, pursuant to Regulation (EU) 2021/2282 on health technology assessment, procedural rules for the interaction during, exchange of information on, and participation in, the preparation and update of joint clinical assessments of medical devices and in vitro diagnostic medical devices at Union level, as well as templates for those joint clinical assessments

German title
Durchführungsverordnung (EU) 2025/2086 der Kommission vom 17. Oktober 2025 zur Festlegung von Verfahrensvorschriften für das Zusammenspiel im Zuge der Erstellung und Aktualisierung gemeinsamer klinischer Bewertungen von Medizinprodukten und In-vitro-Diagnostika auf Unionsebene, den Informationsaustausch darüber und die Beteiligung daran sowie zur Festlegung von Mustern für diese gemeinsamen klinischen Bewertungen gemäß der Verordnung (EU) 2021/2282 über die Bewertung von Gesundheitstechnologien
Publication date
2025-10-17
Original language
German
Pages
41

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Publication date
2025-10-17
Original language
German
Pages
41

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