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 and compares provisions of current legislation. Covers issues related to the reporting and publication...
| 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 and compares provisions of current legislation. Covers issues related to the reporting and publication of clinical trials, including appropriateness/presentation, timing, 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. |