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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.

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