TITLE

QI monitoring forms, tools put compliance checking at fingertips

PUB. DATE
May 2009
SOURCE
Clinical Trials Administrator;May2009, Vol. 7 Issue 5, p57
SOURCE TYPE
Periodical
DOC. TYPE
Article
ABSTRACT
This article focuses on the claim by Julie Ozier, an associate director of the IRB at Vanderbilt University in Nashville, Tennessee that a good compliance program for clinical trials can be built around monitoring tools. Ozier explained that they have started their compliance plan around monitoring tools and the forms and tools they use were interview-based, checking forms, looking at the program, checking source documents and regulatory documents and create a report around them.
ACCESSION #
37811768

 

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