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.
Posts Tagged ‘compliance’
Does Dr. Q need to do anything additional to be in compliance with HIPAA?
Posted: 25th July 2010 by admin in CONFIDENTIAL DRUG REHABILITATIONTags: additional, anything, compliance, HIPAA, need
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