FDA Oversight of the Tissue Bank Industry
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| dc.contributor.advisor |
Hutt, Peter Barton
|
en_US |
| dc.contributor.author |
Wang, Mary H. |
en_US |
| dc.date.accessioned |
2012-06-07T20:45:45Z |
|
| dc.date.issued |
2002 |
en_US |
| dc.identifier.citation |
FDA Oversight of the Tissue Bank Industry (2002 Third Year Paper) |
en |
| dc.identifier.uri |
http://nrs.harvard.edu/urn-3:HUL.InstRepos:8852205 |
|
| dc.description.abstract |
Until recently, FDA oversight of the human tissue industry has been spotty, even nonexistent. However, industry explosion has forced the FDA to not only publish general industry standards in 1993 (finalized in 1997), but to update those standards with more comprehensive rules that are currently being reviewed. Needless to say, lack of adequate funding has proven problematic for the cash-strapped agency in terms of enforcing any regulations the agency hopes to promulgate. |
en |
| dc.language.iso |
en_US |
en |
| dash.license |
LAA |
en_US |
| dc.subject |
Food and Drug Law |
en |
| dc.subject |
human |
en |
| dc.subject |
tissue |
en |
| dc.subject |
industry |
en |
| dc.subject |
banking |
en |
| dc.subject |
oversight |
en |
| dc.subject |
regulation |
en |
| dc.title |
FDA Oversight of the Tissue Bank Industry |
en |
| dc.type |
Paper (for course/seminar/workshop) |
en_US |
| dc.date.available |
2012-06-07T20:45:45Z |
|
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