Recorded March 31, 2015
Learn about biosimilars’ potential impact on the U.S. market and how payers should prepare now.
Although an approval pathway for biosimilars has been available since the Affordable Care Act passed in 2010, the U.S. has yet to see the FDA approve a drug through this process. But the agency has been working with multiple companies that are hoping to finally gain approval for and launch these products, potentially increasing price competition of various biologics. And with an increasing
You must be logged in to post a comment.