GHTF A Boon To Pre-Owned Capital Equipment Market – Commerce Dept.
This article was originally published in The Gray Sheet
Executive Summary
The Global Harmonization Task Force's elevation of refurbished medical supply regulation issues "an important development" in lifting barriers for U.S. manufacturers exporting the devices, according to a Sept. 26 report by the U.S. Department of Commerce
You may also be interested in...
SUD Reprocessing Guidance Retains Premarket Exemptions For Now
FDA has not yet decided whether it will retain premarket exemptions for reprocessed Class I/II single-use devices (SUDs), according to the Aug 2 final guidance "Enforcement Priorities for Single-Use Devices Reprocessed by Third Parties and Hospitals."
Amunix Raises $117m To Take Novel T-Cell Engager Into The Clinic
Amunix’s XTEN technology for half-life extension and precise drug delivery has been used by multiple partners over the past 15 years, but now the firm is building its own cancer therapy pipeline.
Global Medtech Guidance Tracker: February 2021
Stay current on regulatory guidelines from around the world with Medtech Insight's Guidance Tracker. Thirty-eight guidance documents have been posted on the tracker since its last update.
Need a specific report? 1000+ reports available
Buy Reports
Register for our free email digests: