Clinical Trials Reporting and Publication.

Format:

Book

Government document

Author/Creator:

Library of Congress. Congressional Research Service.

Language:

English

Subjects (All):

Medicine--Research.

Medicine.

Product safety.

Publishers and publishing.

Physical Description:

1 online resource (40 pages, digital, PDF file)

Place of Publication:

[Place of publication not identified] : [publisher not identified], 2007.

System Details:

text file

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 goals, appropriateness/presentation, timing, voluntary or mandatory reporting, conflicts of interest, and inclusion of trials related to medical devices.

Notes:

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.

Other Format:

Microfiche version: Library of Congress. Congressional Research Service. Clinical Trials Reporting and Publication

Access Restriction:

Restricted for use by site license.