FDA's response to E-Ferol
Executive Summary
Agency submission for the E-Ferol hearing record should be ready by Sept. 14, Com. Young told House Intergovernmental Relations Subcmte. Chairman Weiss in an Aug. 30 letter. Stating that "We are giving high priority to the outstanding requests" from Weiss, Young said "my target date to respond to your letters on E-Ferol and the submission for the E-Ferol hearing record is Sept. 14." FDA's response to the subcmte.'s reports on Zomax and Oraflex "also should be ready" at that time, Your said
You may also be interested in...
US Q1 Consumer Health Earnings Preview: Label This One Historic And Challenging But Promising
US OTC drug and supplement firms’ reports of results for the first three months of 2024 began on April 19 with P&G. JP Morgan analysts say while “some retailers in the US in particular” are reducing consumer health inventories, for the overall sector they expect “a healthier balance of positive volume and lower pricing contribution.”
Keeping Track: Cancer Approvals From Lumisight Imaging To Adjuvant Alecensa
The US FDA’s approval of Lumicell’s optical imaging agent Lumisight makes a dozen novel approvals in 2024 for the Center for Drug Evaluation and Research.
Partisan Politics Returns To US FDA Congressional Oversight
The US FDA has stood out as an agency that tends to draw broad bipartisan support amid a generally rancorous and divided Congress. A House hearing, however, may be a sign that those days are over.