News|Videos|September 25, 2026

CPHI Milan: USP Benchmarks Reshape Procurement Incentives

Ronald Piervincenzi, USP, explains why manufacturers should act now and how benchmarking could reward reliable generic drug suppliers.

In part 1, of a 3-part interview, Ronald T. Piervincenzi, CEO of the US Pharmacopeia (USP), urges pharmaceutical manufacturers to look past the daily stream of policy headlines and act on the broader push toward drug supply chain resilience.

Piervincenzi, who has led USP since 2014, acknowledges that the current policy environment creates uncertainty for industry. "I think that there is so much news coming in about policy changes and shifts that there's a fear that companies have to maybe not overreact, but they of course don't want to ignore these important factors," he says.

He sees a clear trend toward actiong globally, with effects upstream on manufacturers and downstream on medicine purchasers. "So the goal we have is maybe to not pay attention to every single little piece, but rather look at the broader and take seriously the broader goal to improve the resilience, and then look for those solutions and not wait for others to put the demands, on the industry," Piervincenzi explains.

On cost pressures facing generic drug makers, Piervincenzi says USP concentrates on purchasing incentives, making the case that buyers should pay for resilience. He reports broad support for the idea, but purchasers lack the information and systems to act on it. USP's benchmarking initiative aims to close that gap with transparent tools that show health systems and other large procurers which suppliers deliver reliably over time, so they can preference those products in procurement decisions.

One of these tools comes from the USP Resiliency Center and its Medicine Supply Map, which charts the upstream supply chain for approved US medicines. USP data also show drug discontinuations on the rise, with USP officials calling for clear benchmarks for supply reliability and payment mechanisms that value quality and continuity.


Related to this article

CPHI Milan 2026: Nitrosamine Risk Mitigation, Part 2
Mitigating nitrosamine risk requires assessing each product individually, says Bram Baert, Global Head of Regulatory Affairs at Capsugel, and Sandrine Picco, Senior Analytical Specialist on Capsugel's Innovaform Accelerator Team, in this interview with PharmTech.
PharmTech Weekly Roundup—October 2, 2026
This week on PharmTech, Merck diversified its pipeline, USP emphasizes supply chain security, AI systems are examined, and speakers preview their presentations at CPHI Milan and AAPS PharmSci 360.
CPHI Milan 2026: Nitrosamine Risk Mitigation, Part 1
Capsugel's Bram Baert and Sandrine Picco argue that chasing zero nitrite in pharmaceutical excipients is often impractical and costly. They recommend setting scientifically justified, risk-based limits and consistently staying below them.