| The Regulation of Veterinary Regenerative Medicine and the Potential Impact of Such Regulation on Clinicians and Firms Commercializing These Treatments. | |
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MedLine Citation:
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PMID: 21872766 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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This article provides an overview of the US Food and Drug Administration's current and potential regulation of veterinary regenerative medicine and the various products used in the practice. This article also discusses several of the potential enforcement risks associated with the commercialization of such therapies and products and offers the reader strategies for mitigating those risks. Finally, the article concludes with a review of an important and ongoing court battle that focuses on the marketing and promotion of cellular-based therapies for humans that could have a significant impact on the regulation of both human and veterinary products. |
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Authors:
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Karl M Nobert |
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Publication Detail:
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Type: JOURNAL ARTICLE |
Journal Detail:
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Title: The Veterinary clinics of North America. Equine practice Volume: 27 ISSN: 1558-4224 ISO Abbreviation: - Publication Date: 2011 Aug |
Date Detail:
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Created Date: 2011-8-29 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8511904 Medline TA: Vet Clin North Am Equine Pract Country: - |
Other Details:
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Languages: ENG Pagination: 383-391 Citation Subset: - |
Copyright Information:
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Copyright © 2011. Published by Elsevier Inc. |
Affiliation:
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K&L Gates LLP, 1601 K Street, NW, Washington, DC 20006, USA. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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