tan kesselheim - Search Results

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Year	Number of Results
2013	1
2014	2
2015	1
2020	1
2022	0

Page 1

Implementing U.S. Covid-19 Testing: Regulatory and Infrastructural Challenges.

Tan YT, Kesselheim AS. Tan YT, et al. J Law Med Ethics. 2020 Sep;48(3):606-612. doi: 10.1177/1073110520958889. J Law Med Ethics. 2020. PMID: 33021179 No abstract available.

The roles of academia, rare diseases, and repurposing in the development of the most transformative drugs.

Kesselheim AS, Tan YT, Avorn J. Kesselheim AS, et al. Health Aff (Millwood). 2015 Feb;34(2):286-93. doi: 10.1377/hlthaff.2014.1038. Health Aff (Millwood). 2015. PMID: 25646109

Postmarket surveillance of medical devices: a comparison of strategies in the US, EU, Japan, and China.

Kramer DB, Tan YT, Sato C, Kesselheim AS. Kramer DB, et al. PLoS Med. 2013;10(9):e1001519. doi: 10.1371/journal.pmed.1001519. Epub 2013 Sep 24. PLoS Med. 2013. PMID: 24223035 Free PMC article.

Ensuring medical device effectiveness and safety: a cross--national comparison of approaches to regulation.

Kramer DB, Tan YT, Sato C, Kesselheim AS. Kramer DB, et al. Food Drug Law J. 2014;69(1):1-23, i. Food Drug Law J. 2014. PMID: 24772683 Free PMC article.

Existing FDA pathways have potential to ensure early access to, and appropriate use of, specialty drugs.

Kesselheim AS, Tan YT, Darrow JJ, Avorn J. Kesselheim AS, et al. Health Aff (Millwood). 2014 Oct;33(10):1770-8. doi: 10.1377/hlthaff.2014.0529. Health Aff (Millwood). 2014. PMID: 25288421

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