Posted in:News FDA Reauthorization Bill is Enacted–Changes Biosimilar User Fees and Review Model By Aydin Harston August 4, 2017 Comments are off The U.S. Senate passed S.934 – FDA Reauthorization Act of 2017 on Thursday, August 3, 2017, by a 94-1 vote after having been passed by... Read more Tagged with: BPCIA, BSUFA II, FDA, Guidance, Regulatory http://twitter.com/share?text="[TITLE]&url=[PERMALINK]ShareEmail, Linked In, Twitter, Facebook, Google Plus
Posted in:News Update: BsUFA II Clears the House and Awaits Senate Vote By Aydin Harston and Andrew Storaska July 14, 2017 Comments are off H.R.2430 – FDA Reauthorization Act of 2017, a bill reauthorizing all of the U.S. Food and Drug Administration (“FDA”) user fee... Read more Tagged with: BPCIA, BSUFA II, FDA, Guidance, Regulatory http://twitter.com/share?text="[TITLE]&url=[PERMALINK]ShareEmail, Linked In, Twitter, Facebook, Google Plus
Posted in:Regulatory An Overview of Important Changes in BsUFA II By Aydin Harston June 27, 2017 Comments are off The Biosimilar User Fee Act (“BsUFA”) was originally enacted in 2012, and the current legislative authority is set to expire at the end... Read more Tagged with: BPCIA, BSUFA II, FDA, Guidance, Regulatory http://twitter.com/share?text="[TITLE]&url=[PERMALINK]ShareEmail, Linked In, Twitter, Facebook, Google Plus
Posted in:Regulatory FDA Provides a Snapshot of the Biosimilar Development Programs By C. Nichole Gifford February 8, 2017 Comments are off Dr. Leah Christl, the FDA’s Associate Director for Therapeutic Biologics, Office of New Drugs Therapeutic Biologics and Biosimilars Team... Read more Tagged with: BSUFA II, FDA, Interchangeability, Regulatory http://twitter.com/share?text="[TITLE]&url=[PERMALINK]ShareEmail, Linked In, Twitter, Facebook, Google Plus