FDA Premarket Regulation of Tissue-Engineered Replacement Parts for Humans
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FDA Premarket Regulation of Tissue-Engineered Replacement Parts for Humans
| Title: | FDA Premarket Regulation of Tissue-Engineered Replacement Parts for Humans |
| Author: | Leon, Doraliz |
| Citation: | FDA Premarket Regulation of Tissue-Engineered Replacement Parts for Humans (2003 Third Year Paper) |
| Full Text & Related Files: |
Ortizdeleon.pdf (209.9Kb; PDF) 
Ortizdeleon.rtf (155.0Kb; RTF file) 
Ortizdeleon.html (135.8Kb; HTML)
|
| Abstract: | This paper is a description of tissue-engineered products, their potential for replacing conventional approaches to missing or failing tissues and organs, and FDA’s ongoing efforts to develop a comprehensive and uniform scheme for regulating them. |
| Terms of Use: | This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA |
| Citable link to this page: | http://nrs.harvard.edu/urn-3:HUL.InstRepos:8965598 |
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HLS Student Papers
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