· 2016
Regulation (EU) 2015/848 of the European Parliament and of the Council
- 539citations
- 2016year
Short summary
EU Regulation 2021/2282, applicable from January 12, 2025, aims to ensure the smooth functioning of the internal market for medicines, medical devices, and in vitro diagnostic medical devices.
AI-generated from the title and abstract; the full text is not read.
Key points
- Regulation (EU) 2021/2282 concerns health technology assessment.
- It aims to ensure the proper functioning of the internal market.
- The regulation covers medicines, medical devices, and in vitro diagnostic medical devices.
- It will be applicable from January 12, 2025.
AI-generated from the title and abstract; the full text is not read.
Abstract
A 22 de dezembro de 2021, foi publicado o Regulamento (UE) 2021/2282 do Parlamento Europeu e do Conselho relativo à avaliação das tecnologias da saúde, que visa o bom funcionamento do mercado interno no que diz respeito aos medicamentos, aos dispositivos médicos e aos dispositivos médicos para diagnóstico in vitro. Este regulamento será aplicável a partir de 12 de janeiro de 2025. Em seguida, é apresentado um resumo do documento, o qual se encontra disponível em: https://eur-lex.europa.eu/legal-content/PT/TXT/?uri=CELEX:32021R2282
The authors' abstract, as published at the source., 2016 · DOI ↗
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Field: Law
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