Publications: Katie Kortbein
August 10, 2026
Comments to USTR Regarding Its Section 301 Investigation of Germany’s Persistent Underpayment for Innovative Pharmaceutical Products
Instead of copying other OECD countries in a “reference-price-race-to-the-bottom,” U.S. policy should instead encourage peer countries to appropriately value innovative medicines.
July 22, 2026
The FDA Should Not Allow Untested Peptides to Be Added Into Patients’ Medications
The FDA is considering allowing seven unapproved peptides—substantially sourced through a Chinese gray market—to be used by U.S. compounding pharmacies, despite its own scientists warning against it. Approving them would legitimize unvetted foreign suppliers and undermine evidence-based drug regulation.
