No Ordinary Subjects
Welcome to 'No Ordinary Subjects,' a new health, medicine, and clinical research-focused podcast with a mission of shining a bright light on overlooked issues and underrepresented perspectives. Here, we aim to explore the facets and implications of diversity, equity and inclusion from the perspectives of all stakeholders. From those providing care across specialties, to individuals working tirelessly to bring new therapies to market, and the medical heroes who decide to participate in clinical trials. Whether patients or healthy volunteers— just don't call us "subjects!" Guests are the extraordinary humans in every sector of this ecosystem who are making progress possible for the rest of us. Join me on this collective journey toward better outcomes — for ALL. Feedback and suggestions for podcast topics and guests are welcome! Please share the links with those you care about, and subscribe to catch every episode on your favorite platform. Thanks in advance! #beyondlipservice
No Ordinary Subjects
Guidance with Teeth - Why the FDA Needs Enforcement Power
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In this episode of No Ordinary Subjects, host Allison Kalloo exposes a critical flaw in how clinical trials are regulated in the U.S. The FDA can issue guidance, make recommendations, and encourage diversity— but it lacks the power to enforce meaningful change. Without Congressional action, clinical trial sponsors can continue treating inclusion as optional. It’s time to demand more than suggestions. Tune in for a frank discussion on why the FDA needs real authority and what’s at stake if we keep accepting business as usual. Read the companion article on LinkedIn.
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