Washington Policy Briefing on FDA and Other Regulatory Updates

March 03, 2026
As PDUFA VIII negotiations begin and on-going debates on the best way to ensure patients can access medicines continue, biotech executives and investors are seeking clarity on how policy will impact their operational and investment decisions. Leaders from BIO and Washington policy and regulatory experts will share insights on what is known about developments at FDA, CMS, HHS and briefings with elected officials to create a policy and regulatory environment that leads to the shared goal of the best health outcomes for patients.
Speakers
Anna Abram
Anna Abram, Senior Advisor, Health Care Policy and Legislation - Akin
Crystal Kuntz
Crystal Kuntz, Senior Vice President, Health Policy & Research - Biotechnology Innovation Organization (BIO)
Jim Meyers
Jim Meyers, Senior Advisor - Boston Consulting Group (BCG)
Carl Schmid
Carl Schmid, Executive Director - HIV+Hepatitis Policy Institute