FDA Panel Discusses Extreme Weather’s Effect On Medical Device Availability
This article was originally published in The Gray Sheet
Executive Summary
FDA’s Device Good Manufacturing Practice Advisory Committee met April 11 to help the agency develop better policies to prepare for and respond to extreme weather conditions that impact medical devices.
You may also be interested in...
FDA Examines Extreme Weather Impact On Device Supply Chains
The agency called an advisory committee meeting and public comment period to collect feedback from device firms and others on effects that extreme weather and natural disasters pose to medical device safety and quality.
HHS Innovation Project To Develop More Resilient DME For Natural Disasters
Over the next six to 12 months, a team working through HHS’ Innovation Fellows Program will develop medical technology capable of withstanding natural disasters.
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.”