Device CEOs Fear New FDA Resources Will End Up On Food’s Plate
This article was originally published in The Gray Sheet
Executive Summary
With congressional scrutiny of food safety at an all-time high, medical device executives are worried that FDA's newfound resources will be diverted from devices toward the food sector
You may also be interested in...
510(k) Process Issues Surface At FDA Appropriations Hearings
Deputy FDA Commissioner Joshua Sharfstein told Congress he and incoming Commissioner Margaret Hamburg will be taking a look at the 510(k) clearance process to determine whether it is truly flawed, or just misunderstood
Obama Budget Would Boost FDA Device Program Funding 12.5%
The Obama administration's fiscal year 2010 budget request includes a $35 million funding increase for FDA device programs
New EU Approvals
The Pink Sheet's list of EU centralized approvals of new active substances has been updated to add two new products, including Ryzneuta, Evive Biotechnology's treatment for chemotherapy-induced neutropenia.