A Transforming Industry Needs a Reimagined Event
This year’s edition of CPHI Americas represents far more than an incremental improvement over previous years. Moving beyond the traditional trade show format, our upcoming show is driven by a specialized focus on contract manufacturing, ensuring every aspect of programming, networking, and content delivers maximum relevance and business value to the CDMO and CMO community. This evolution comes in direct response to the industry's shifting dynamics; the rise in outsourcing has created an ecosystem where CDMOs, CMOs, biotech innovators, regulatory experts, investors, private equity groups, and technology partners must collaborate more closely than ever before.
CPHI Americas 2026 positions itself at the center of this ecosystem, providing the platform where these critical relationships can be formed, strengthened, and leveraged for mutual success. With over 295 exhibitors, 3,700 attendees, and 80+ industry thought leaders confirmed for this year’s show, you’ll get unparalleled access to the decision-makers, innovators, and experts shaping the future of pharmaceutical manufacturing in the Americas.
Content That Tackles the Issues Keeping You Up at Night
One of CPHI Americas’ most distinctive features is its commitment to addressing the controversial, complex issues that pharmaceutical professionals genuinely grapple with, with three days of discussions which ask the difficult questions and demands actionable answers.
Featured content tracks include:
The CDMO Panel: Last year’s most popular lunch session returns, bringing together the biggest players in contract manufacturing for candid discussions about market dynamics, capacity constraints, technology investments, and partnership strategies. Forget corporate polish and sugarcoating, this is real talk from industry leaders about the challenges and opportunities shaping the CDMO landscape.
Government & Regulatory Insights Track: In an environment where regulatory shifts can derail development timelines and impact market access, direct access to regulatory thinking provides invaluable strategic intelligence. This track showcases experts from the FDA and other regulatory authorities, this track addresses the daily changes in compliance requirements, onshoring incentives and requirements, AI oversight and validation, and evolving quality standards.
The Hot Seat: These high-energy, moderated panels tackle controversial industry issues head-on, from onshoring incentives and their practical implications to pricing transparency debates and global supply chain dependence. The format encourages frank discussion and diverse perspectives, moving beyond consensus positions to explore the tensions and trade-offs that characterize real-world decision-making.
The speaker lineup reflects this commitment to substantive content. Over 80 industry thought leaders, including voices from the FDA, will share insights, challenge assumptions, and facilitate discussions that advance industry thinking. Notable speakers include Richard Pazdur, Sirsij Peshin, Mike Martin, Molly Klote, Mayank Nagar, Derek Booth, Nishtha Jain, Luiz Barberini, Daniel Cohen, and John Nosta, founder of NOSTALAB and author of The Borrowed Mind, who will conduct a book signing on June 3, 2026.