The FDA has released its report “FDA Report on the Quality, Safety, and Effectiveness of Servicing of Medical Devices In accordance with Section 710 of the Food and Drug Administration Reauthorization Act of 2017 (FDARA).”
Author: TechNation Magazine
The HTMA-OH will hold a Spring Regional Meeting on Wednesday, May 16 beginning at 4:30 p.m.
The FDA announced that it intends to replace the Quality System Regulation (21 CFR 820) with the specifications found in the international quality management standard ISO 13485:2016.
This 60-minute webinar provided an overview of X-ray quality assurance by looking at how technology has driven efficiency over the past 20 years.
BC Biomedical’s ESU-2400H Electrosurgical Unit Analyzer’s DFA2 Technology is now patented under U.S. Patent No. 9,883,903.
In this webinar, attendees learned what to look for as well as information about the newest technology and best-practices for proactive probe testing.
Two companies that help facilities achieve operational mandates within different operational areas have integrated their respective online tools.
Global Medical Imaging (GMI), soon to be Avante Ultrasound, has received its certificate of registration to the Medical Devices Quality Management Standard of ISO 13485:2016.

