The U.S. Food and Drug Administration (FDA) is announcing a webinar to discuss the Cybersecurity in…
Author: TechNation Magazine
Rep. Neal Patrick Dunn (R-Florida) recently provided insightful testimony regarding H.R.7253 – Clarifying Remanufacturing to Protect…
In its continued efforts to harmonize with international regulatory authorities, the U.S. Food & Drug Administration has announced its intention to amend the current good manufacturing practice requirements of the FDA quality system regulation, 21 C.F.R 820 et seq. to align more closely with the international consensus standard for devices, ISO 13485.
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A U.S. national BMET Apprenticeship Program recently launched by AAMI has gained a valuable new employer…
The recent Webinar Wednesday session “HTM Professionals’ Role on a Patient Safe Endoscope” was presented by…
Danielle McGeary joins MultiMedical System’s Chyrill Sandrini, to discuss the next generation for clinical engineering; addressing the current demographics, based on a survey conducted by AAMI, and what we can expect to see in the next 15 years.
PartsSource, an online marketplace for medical equipment maintenance parts and services, has announced updates to PartsSource…

