09/16/2026
As the FDA marches toward the likely first approval of a psꪗchꫀdeꪶic medicine, the agency convened a hearing on September 14th seeking public input on how these drugs should be used, monitored and continuously studied in the real world.
The biggest question swirling around the hearing was one of access. Should a psꪗchꫀdeꪶic medicine be approved, who would the FDA allow to administer it? And how would that decision impact patients’ ability to actually receive the treatment?
NCPM President Jon Dalton testified before the FDA, bringing a distinctly Nevada perspective to the national conversation. He highlighted one of the most important barriers to equitable access: the shortage of qualified providers and clinical capacity in rural and frontier communities. Jon urged the FDA to preserve an appropriate role for trained non-physician clinicians and to develop product-specific safety requirements that reflect the realities of local healthcare systems.
Submit Written Comments:
Written comments must be submitted to the Federal Register : Considerations for Potential Future Therapeutic Use of Psꪗchꫀdeꪶic Drugs; Public Hearing; Request for Comments electronic filing system on or before 11:59 p.m. ET on October 5, 2026. Link in bio!
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