Clinical Trials Hipaa
by admin on Thursday, August 19th, 2010 | Comments Off
clinical trials hipaa
Does Dr. Q need to do anything additional to be in compliance with HIPAA?
Dr. Q received IRB approval to conduct a clinical trial at Hospital Z to test drug A vs. drug B on October 31, 2001. Subject recruitment has been completed however, due to an adverse event on May 3, 2003, the IRB requested that the principal investigator re-consent subjects.
I think it depends on the adverse event.. was the event like someone broke in and stole all of the consent forms or Dr.Q’s ID#/Name list?
That sounds about right though.
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HIPAA in Clinical Trials: A Practical Guide for Research Compliance $99.50 An easy-to-read resource guide describes the HIPAA privacy regulations as they apply to research. Includes case scenarios, samples of policies and procedures, and plain-English interpretations of regulations. Detailed information on authorization and pre-screening processes as they pertain to research. CD-ROM included. Softcover…. |
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HIPAA Training Handbook for Researchers PKG: HIPPA and Clinical Trials $57.10 … |
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‘De-identifying’ information could help make HIPAA bite less; other means suggested. (HIPAA).: An article from: Bioresearch Monitoring Alert $5.95 This digital document is an article from Bioresearch Monitoring Alert, published by Washington Information Source on February 1, 2003. The length of the article is 1993 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.Cit… |
