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Informed Consent Process Trips Up Many Clinical Registries – Consultant

This article was originally published in The Gray Sheet

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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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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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