Audit clinical trials to prevent patient safety violations
Health Care Auditing Strategies, November 1, 2005
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Editor's note: This is the second in a two-part series.
If you want to hunt down patient safety noncompliance in clinical trials, it's difficult to know where to look first.
However, there are a few areas that can serve as good diving-off points, says Tamara J. O'Black, CIP, regulatory affairs administrator for Park Nicollet Institute in Minneapolis.
In the second in a two-part series, O'Black offers strategies for auditing the patient safety aspect of clinical trials. This is a follow-up discussion from last month, when HCAS discussed strategies for auditing the billing component of clinical trials.
This is an excerpt from a member only article. To read the article in its entirety, please login.
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