The Congressional Personalized Medicine Caucus and the Personalized Medicine Coalition co-organized a Congressional briefing on February 26, 2020, titled "Technologies Advancing the Future of Personalized Medicine."
The Congressional Personalized Medicine Caucus and the Personalized Medicine Coalition co-organized a virtual Congressional briefing on June 30, 2020, titled "The Personalized Medicine Community's Response to COVID-19."
The Congressional Personalized Medicine Caucus and the Personalized Medicine Coalition co-organized a virtual Congressional briefing on April 28, 2022, titled "Promoting Innovation and Delivery of Cell and Gene Therapies."
At the United States Capitol on December 5, the co-chairs of the Congressional Personalized Medicine Caucus organized a briefing in cooperation with the Personalized Medicine Coalition to help educate their colleagues in the House and Senate about the importance of adopting public policies designed to alleviate educational, reimbursement, and clinical adoption challenges that make it difficult for clinicians to take full advantage of emerging opportunities in personalized medicine. The briefing featured remarks from leaders in academia, patient advocacy, and the diagnostics industry.
On May 24, 2023, PMC convened an audience of journalists, policymakers, and business leaders at the National Press Club in Washington, DC, where National Human Genome Research Institute (NHGRI) Director Eric Green delivered the Coalition's Annual State of Personalized Medicine Address on the past, present, and future of the field.
A meeting of PMC's Public and Science Policy Committees will take place on June 28, 2023, from 12:00 - 2:00 p.m. ET in Washington, DC. PMC members will receive details and a registration link via email.
Alexion/AstraZeneca Rare Disease, the EveryLife Foundation for Rare Diseases, the National Society of Genetic Counselors, and the Personalized Medicine Coalition will convene a reception with Congressional leaders and rare disease experts on Tuesday, July 18, at 5:30 p.m. to discuss how Congress, patient advocates, and industry leaders can work together to deliver faster diagnoses for rare disease patients. The reception will take place in Room 2322 of the Rayburn building. RSVP to Gwen Fuller at gfuller@forbes-tate.com.
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