New FDA Policies for Faster Drug Reviews Met with Mixed Reactions · Meenakshi Prabhune, PhD
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While many in the biotechnology sector expressed excitement for faster drug approval timelines, some researchers voiced concerns that critical data review could be missed. BY SHELBY BRADFORD, PhD I n July 2025, the US Food and Drug Administration (FDA) announced a pilot program intended to expedite reviews for drug applications that met one of five national priorities, including products deemed “innovative breakthrough therapies” or therapies that target a “large unmet need.” The program, the Commissioner’s National Priority Voucher (CNPV), aims to decrease the timeline of reviews, which are currently from six to eight months, to between one and two months. …
摘自《科学家》(The Scientist)第40卷 第2期 · 2026年夏季刊,Meenakshi Prabhune, PhD。仅引用开头一小段供了解文章,版权归原刊所有,全文请阅读原刊。