Medical Device Legislation
"Medical Device Legislation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Laws, statutes, and regulations pertaining to devices used in medicine.
Descriptor ID |
D062307
|
MeSH Number(s) |
N03.706.615.473.500
|
Concept/Terms |
Medical Device Legislation- Medical Device Legislation
- Device Legislation, Medical
- Device Legislations, Medical
- Legislation, Medical Device
- Legislations, Medical Device
- Medical Device Legislations
- Medical Equipment Legislation
- Equipment Legislation, Medical
- Equipment Legislations, Medical
- Legislation, Medical Equipment
- Legislations, Medical Equipment
- Medical Equipment Legislations
Medical Device Regulation- Medical Device Regulation
- Device Regulation, Medical
- Device Regulations, Medical
- Medical Device Regulations
- Regulation, Medical Device
- Regulations, Medical Device
|
Below are MeSH descriptors whose meaning is more general than "Medical Device Legislation".
Below are MeSH descriptors whose meaning is more specific than "Medical Device Legislation".
This graph shows the total number of publications written about "Medical Device Legislation" by people in this website by year, and whether "Medical Device Legislation" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2018 | 0 | 1 | 1 |
2019 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
2021 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Medical Device Legislation" by people in Profiles.
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Easing Medical Device Regulatory Oversight: The FDA and Testing Amidst the COVID-19 Pandemic. Am J Law Med. 2021 07; 47(2-3):291-326.
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Evaluating the safety and effectiveness of novel personal protective equipment during the COVID-19 pandemic. Med J Aust. 2021 06; 214(11):496-499.e1.
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Does Trypsin Oral Spray (Viruprotect®/ColdZyme®) Protect against COVID-19 and Common Colds or Induce Mutation? Caveats in Medical Device Regulations in the European Union. Int J Environ Res Public Health. 2021 05 11; 18(10).
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How the European in vitro diagnostic regulation could negatively impact the European response to the next pandemic: an urgent call for action before May 2022. Clin Microbiol Infect. 2021 08; 27(8):1074-1075.
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The medical right to repair: the right to save lives. Lancet. 2021 04 03; 397(10281):1260-1261.
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Australian Medical Device Regulation during COVID-19: Has the Australian Regulatory Framework for Medical Devices Been Effective during the COVID-19 Pandemic? J Law Med. 2021 Mar; 28(3):745-759.
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Medical Device Regulation: Requirements for Dental Professionals Who Prescribe and Manufacture Custom-Made Devices. Prim Dent J. 2021 Mar; 10(1):64-88.
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Regulatory Agilities in the Time of COVID-19: Overview, Trends, and Opportunities. Clin Ther. 2021 01; 43(1):124-139.
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COVID-19: Regulatory Landscape of Medicinal and Medical Device Products for Human Use. Clin Ther. 2020 08; 42(8):1444-1450.
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COVID-19 and respiratory support devices. Paediatr Respir Rev. 2020 Sep; 35:61-63.