the deputy commissioner for human foods at the FDA, said during a Senate meeting this week, per NBC. According to the FDA, the agency has reviewed the safety of Red 3 —which is derived from ...
Acelyrin (NASDAQ:SLRN) shares traded higher on Friday after the company scheduled an investor meeting for next week to ...
On Sept. 25, the U.S. Food and Drug Administration (FDA) hosted a public meeting to gather feedback on its proposed framework ...
A discussion of the development of consumer protection law in the US through the enactment of key legislation and formation ...
The FDA’s decision will close a lucrative market opportunity for compounding pharmacies, although the agency will give a ...
MannKind expects to submit a request for a supplemental new drug application (sNDA) meeting with the U.S. Food and Drug Administration (FDA) in 1H 2025 to discuss the data and filing timeline.
On December 17, 2024, the Company conducted a Submission Issue Request (SIR) meeting with the FDA. Management believes its comprehensive plans to address the Additional Information Request (AIR ...
Kazia Therapeutics updates paxalisib's regulatory progress after FDA discussions on glioblastoma data, highlighting plans for ...