
Doug Bain, founder and consulting partner of ClinFlo, discusses his proposed regulatory blueprint for digital trials in the latest episode of The Scope of Things podcast. With host Deborah Borfitz, Bain delves into his strategy for turning 21 CFR Part 11 into a more practical regulation that streamlines rather than bogs down clinical trials, what would qualify someone to take on the role as a trusted third party (and what makes them trustworthy), and the new FDA administration’s modernization...
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Episode: 51 - Bridging the Equity Gap in Oncology with Eugene Manley, Jr.

Episode: 50 - Ramona Burress and Cassandra O’Neal on Health Equity That Works

Episode: 49 - Mike Sullivan on AI and Clinical Operations in the Year 2030

Episode: 48 - Florence Mowlem on the Challenges and Solutions of Pediatric Rare Disease Trials
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