Software is playing an expanding role in modern medical devices, raising the question of how developers, regulators, medical professionals, and patients can be confident in the devices' reliability, ...
Kimberlee Leonard has 22 years of experience as a freelance writer. Her work has been featured on US News and World Report, Business.com and Fit Small Business. She brings practical experience as a ...
In follow-up to our colleagues recent post about the newly implemented Medical Device Regulation (“MDR”) in the European Union, this post will discuss some of the similarities between FDA’s Clinical ...
New capability allows for central management of process instrumentation using a Rockwell Automation PlantPAx process automation system or an existing automation system Rockwell Automation has added ...
In-house and private practice counsel set out the challenges and opportunities of protecting software in medical devices and software as a medical device Medical device manufacturers have been ...
End Users Request A Technology that Provides One Software Tool, Integrating Device Assets Over the years end users have requested a single technology that provides one software tool to integrate ...
FDT-compatible tools simplify integration and network scanning. Endress+Hauser’s stand-alone engineering software interface, FieldCare (FDT Frame Application), has been updated to Version 2.10. The ...
The FDA recently released six guidance documents as part of the agency’s continued focus on updating the regulatory stance on software as a medical device and other digital health products. The ...
Microsoft’s System Centre Configuration Manager (SCCM) and Active Directory (AD) registration is required for all corporate desktops to support cybersecurity needs. SCCM provides remote management ...
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