Skip to Primary Navigation

FDA to streamline biosimilar development to lower drug prices

A photo of a worker in mask and white doctor's jacket in a drug production facility.
Photo: Uriel Sinai/Getty Images

New federal guidance recommends using drugs approved outside of the US as comparators to cut down on pricey pharmacokinetic testing.

According to the US Food and Drug Administration (FDA), new guidance from the regulator could save biosimilar developers up to 50% of their pharmacokinetic (PK) study costs, or approximately $20m.

As part of an effort to lower drug costs, the FDA has made an announcement to facilitate the development of proposed

Get full access, free for a month

Start your 28-day free trial to continue reading and access
all content on GRIP – no payment details required.

What’s included:

  • Every new article, plus our 5,000+ archive
  • Daily regulatory insight and guidance
  • Exclusive interviews and in-depth analysis
  • Coverage of industry-leading events and conferences
  • All podcasts and videos, featuring industry experts
  • The full set of Rules Navigator tools
  • An ad-free experience