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210907 r ||| eng |
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|a Gelband, Hellen
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|a A report on the sponsors of cancer treatment clinical trials and their approval and monitoring mechanisms
|h Elektronische Ressource
|c Hellen Gelband ; prepared for the National Cancer Policy Board
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|a Washington D.C.
|b National Research Council
|c 1999, 1999
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|a Includes bibliographical references
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|a Neoplasms / therapy / https://id.nlm.nih.gov/mesh/D009369Q000628
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| 653 |
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|a United States / https://id.nlm.nih.gov/mesh/D014481
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| 653 |
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|a Clinical Trials as Topic / standards / https://id.nlm.nih.gov/mesh/D002986Q000592
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|a National Cancer Policy Board (U.S.)
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|a eng
|2 ISO 639-2
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| 989 |
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|b NCBI
|a National Center for Biotechnology Information
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|a Title from caption (viewed June 14, 2001). - "February 1999.". - Mode of access: Internet
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|u http://www.nap.edu/catalog.php?record_id=9442
|3 Volltext
|n Provider site
|3 Volltext
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|u https://www.ncbi.nlm.nih.gov/books/NBK224011
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a This report for the National Cancer Policy Board (NCPB) describes the procedures currently in place in the United States for approving and monitoring clinical trials of cancer treatments. Virtually all cancer clinical trials are funded by agencies of the federal government or the pharmaceutical industry, so the focus is on the requirements for each of these groups. The paper is intended as a jumping off point for the NCPB to consider some of the pressing policy issues surrounding clinical trials in cancer, though as yet, no specific follow-on projects have been initiated
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