Informed Consent Process Trips Up Many Clinical Registries – Consultant

This article was originally published in The Gray Sheet

15 Sep 2008
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Executive Summary

Underestimating the importance of the patient informed consent process is a common and costly mistake made by sponsors of medical device registries, according to Jeremy Tinkler, director of regulatory affairs at consulting firm MedPass International

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Informed Consent Process Trips Up Many Clinical Registries – Consultant

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