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Webinar: FDA Fallout & the Future
In a climate of regulatory transformation, uncertainty at the FDA is reshaping the life sciences landscape. Shifting FDA priorities, reduced agency resources, and structural realignments introduce growing ambiguity around approval timelines, enforcement priorities, and post-market expectations.
ELIQUENT’s webinar series – “FDA Fallout & the Future” – explores how life sciences organizations can remain agile, proactive, and inspection-ready amid regulatory uncertainty. With decades of collective experience across regulatory, quality, and safety functions, our team of regulatory leaders and industry experts will share their unique insights and pragmatic solutions to adapt and plan for what’s ahead.
Whether you’re preparing for upcoming submissions, navigating post-market changes, or building resilience into your regulatory operations—this series is designed to help you respond with confidence.
Meet the Panel
With years of experience at the FDA and within regulated industry, our panel of ELIQUENT Experts bring a unique, insider perspective to the complex transitions shaping the agency. Having worked on regulatory policy, enforcement, and industry compliance, they’ve seen firsthand how leadership and regulatory shifts impact FDA priorities, approvals, and oversight.
Their deep institutional knowledge, combined with real-world industry insights, allows them to break down these changes in a way that’s both informative and actionable for stakeholders navigating this evolving landscape
John Taylor, JD
More than 30 years of global leadership in the life sciences industry including roles as a senior FDA official acting in multiple high-profile positions at the Agency and leadership roles within industry.
Learn more about John
Brian Mayhew, MA, MBA
More than 25 years of regulatory policy experience in the life sciences industry, including roles in the FDA’s Office of the Commissioner and senior positions throughout industry.
Learn more about Brian
Wendy Sanhai, PhD, MBA
Distinguished life sciences leader, scientific expert, and member of ELIQUENT’s Board of Directors with experience that spans senior roles at FDA and NIH, academia, and regulated industry.
Learn more about Wendy
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Stay Informed
Interested in learning more about the profound changes occurring within the FDA and the broader regulatory landscape during President Donald Trump’s second term? Join us as we engage with former FDA senior officials, policy experts, and industry leaders to provide firsthand insights into how these transitions are reshaping the FDA and the industries it regulates.
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