CDRH REINVENTION RECOMMENDATIONS FROM INDUSTRY SOUGHT BY BURLINGTON; FDA TASK GROUPS BEING FORMED TO DEVELOP DEVICE CENTER RATIONALIZATION PLAN
This article was originally published in The Gray Sheet
Executive Summary
Device industry input on ways to "rationalize" FDA device center programs is being sought by Center for Devices and Radiological Health Director Bruce Burlington. Manufacturers' suggestions will be taken into account as CDRH develops a plan for revamping its operations in response to a tight budget.
You may also be interested in...
Kenvue Breaks Ground On New Headquarters, Appoints Chief Corporate Affairs Officer
Firm hosts groundbreaking for 290,000 square-foot global headquarters it’s having built in Summit, NJ, starting with 100,000 square-foot science and innovation and expected to open in 2025. It announced adding Russell Dyer as chief corporate affairs officer starting 13 March.
Xaira Launches With $1bn-Plus And End-To-End AI Strategy
ARCH and Foresite incubated the company and recruited Genentech R&D veteran Marc Tessier-Lavigne to keep data generation, machine learning research and drug development under one roof.
‘Clear’ Is In The Eye Of The Beholder, New York, CRN Argue In Age-Restricted Sales Litigation
CRN’s request for clarification, as it continues litigating complaint in US District Court for Southern New York, highlights what it contends is vague and overly general language in the legislation passed in October with a 22 April effective date.