The MDR’s Usability Requirements

Rules, regulations, and legislations are very necessary to keep the processes running smoothly. The EU has proposed its new Medical Device Regulations (MDR) replacing the old Medical Device Directive (MDD) although the implementation of MDR has been postponed till 26th May, 2022. The MDR proposes several usability requirements for the…
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Medical Device Software & SaMDs: A Crash Course

When it comes to evolution, the technology always has the lead. With new ideas emerging nearly every day on the face of the world, technology keeps reshaping our lives, and innovations and software applications are one prime example of that. Whether it is economic, social, educational, or medical, software programs…
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