New regulation on medical devices made of substances: Opportunities and challenges for pharmacological and toxicological research
The Medical Device (MD) Regulation EU 2017/745 (MDR) has provided a completely new and more robust regulatory framework at guarantee of the safety and efficacy of therapeutic options accessing the market. At the same time, the MDR poses several challenges for stakeholders, among which, the most sign...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Frontiers Media S.A.
2022-09-01
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| Serija: | Frontiers in Drug Safety and Regulation |
| Teme: | |
| Online dostop: | https://www.frontiersin.org/articles/10.3389/fdsfr.2022.1001614/full |
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