ECRI and oneSOURCE announce collaboration to improve medical device alerts management
This article was created by oneSOURCE (now part of RLDatix) and moved from the previous oneSOURCE website. OneSOURCE is now known as Manufacturer Guidelines.
February 23, 2021 — PLYMOUTH MEETING, PA—ECRI, the nation’s largest patient safety and independent device evaluation organization, and oneSOURCE Document Management Services, an RLDatix company and leading healthcare management solution, announce a joint collaboration focused on improving medical device safety and responsiveness of healthcare facilities.
