Drug makers would have to inform FDA about business decisions that could result in drug shortages, under legislation introduced Feb. 7 by Sens. Amy Klobuchar, D-Minn., and Robert Casey, D-Pa.
Join thousands of industry professionals who rely on Pink Sheet for daily insights
Already a subscriber?
Ensitrelvir, Shionogi's treatment for COVID-19, is among the latest products that have been filed for review by the European Medicines Agency for potential EU marketing approval.
AbbVie didn’t get everything it sought from a citizen petition but may still have the upper hand over smaller rivals after FDA gives makers of animal-derived thyroid medications a year to seek approval. If the agency removes compounded products, it could face more pricing pushback.
The findings are consistent with some other research and likely are due to obesity patients becoming more connected to needed health care services.
