As of January 10, 2025, the procedure for manufacturers to report, anticipate, and manage shortages of medical devices and in-vitro diagnostic medical devices has changed once again. It is now harmonized at the European level.
As of January 10, 2025, the procedure for manufacturers to report, anticipate, and manage shortages of medical devices and in-vitro diagnostic medical devices has changed once again. It is now harmonized at the European level.