“Ethics, Quality and Human Safety in Clinical Trials: The Role of the IRB in Medical Device Studies” is the topic of an upcoming lecture by Gretchen Bowker, Pearl Pathways COO and Co-Founder, for Purdue University. The two-day event, April 8-9, is held at Roche and will cover current industry perspective on devices and diagnostics. This course will provide excellent sharing and learning for Purdue students participating.
Single IRB – A Guide to the Common Rule sIRB Mandate
The sIRB requirement is active. Is your study affected?
Clinical Research Accelerated
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