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Posted by John Lehmann on Fri, Jan 22, 2016

A Question of Disclosure: FDA Findings and Publications

When the Food and Drug Administration (FDA) identifies significant findings with the conduct of a clinical trial during an inspection, what happens to those findings? According to a article published online by JAMA Internal Medicine, those findings remain hidden in plain sight.

Charles Seife, MS, a professor at the Arthur L. Carter Institute of Journalism at New York University, conducted a research study that sought to “identify published clinical trials in which an FDA inspection found significant evidence of objectionable conditions or practices, to describe violations, and to determine whether the violations are mentioned in the peer-reviewed literature.”

Topics: Charles Selfe, FDA Warning Letters, FDA Inspection

Posted by John Lehmann on Tue, Aug 25, 2015

Trust the Process – A Case Study

Merriam Webster defines a case study as a published report about a person, group, or situation that has been studied over time; also : a situation in real life that can be looked at or studied to learn about something.  Case studies can be useful to help highlight how to handle a particular situation, including the eventual outcome.

Topics: FDA Audit, FDA Inspection, BIMO

Posted by Brandy Chittester on Wed, Mar 04, 2015

Case Study: Medical Device FDA Inspection

With the trials IMARC Research has monitored, our experience has been that the FDA has begun inspecting clinical sites after the Sponsor submits their Premarket Approval Application (PMA), the application submitted to the FDA for approval of a Class III device. However, on one of the projects we were working on FDA contacted one of the sites for a routine inspection months before the PMA was to be submitted.

Topics: Medical Device, Premarket Approval Application, FDA Inspection

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