Clinical Trials Reporting and Publication.
Reviews Federal regulations, international standards, and recommendations from medical industry organizations regarding drug and medical device clinical trials reporting and publication. Discusses provisions of S. 470 and S. 3196, both the Fair Access to Clinical Trials Act; and covers issues relate...
| Corporate Authors: | , |
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| Format: | eBook |
| Language: | English |
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[Place of publication not identified] :
[publisher not identified],
2007.
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| Series: | U.S. Congressional Research.
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| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
| Summary: | Reviews Federal regulations, international standards, and recommendations from medical industry organizations regarding drug and medical device clinical trials reporting and publication. Discusses provisions of S. 470 and S. 3196, both the Fair Access to Clinical Trials Act; and covers issues related to the publication of clinical trial results, including goals, appropriateness/presentation, timing, intellectual property, voluntary or mandatory reporting, conflicts of interest, and inclusion of trials related to medical devices. |
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| Item Description: | Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Dec. 2010). Reuse except for individual research requires license from ProQuest, LLC. CRS Report. Electronic resource. |
| Physical Description: | 1 online resource. |