As the prospect of import tariffs and drug price reform marshals billions of biopharma investment dollars into the U.S., the feasibility of rapid domestic manufacturing buildouts could hinge on a new program cooking at the FDA. How that program, dubbed PreCheck, will work in practice—and on what timeline—are key questions as the U.S. looks to bolster its local pharmaceutical production base.

This week on “The Top Line,” we dive into comments from a recent public meeting on the industry’s hopes for PreCheck, which is being designed to streamline the process by which new biopharma manufacturing facilities are built in the U.S.

Fierce Pharma’s Fraiser Kansteiner sits down with Christopher Shilling, chief regulatory officer at gene therapy CDMO Forge Biologics—who attended the meeting—to offer an on-the-ground perspective and explore the aspects of the plan that could have the biggest impact on manufacturers. Shilling also outlines what he sees as FDA’s next steps, plus regulatory considerations that could most benefit CDMOs and the broader industry.

To learn more about the topics in this episode: 

• Amid tariff-fueled onshoring push, Trump signs order to boost US stockpiling of certain drug ingredients
• FDA launches generics pilot program, advances facility PreCheck proposal in bid to incentivize US drug manufacturing
• Amid pharma's US investment spree, FDA unveils new program to streamline domestic plant build-outs
• Trump signs executive order to boost US drug manufacturing amid threat of tariffs

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