Vivani Medical Cofounder and CEO Adam Mendelsohn, Ph.D. discusses the company’s first application of the NanoPortal, ...
Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the ...
In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product quality, operational efficiency, and patient safety. Shift from a reactive ...
The rapid evolution of telehealth is transforming how patients access — and physicians provide — care, a shift accelerated by policy changes adopted during the COVID-19 pandemic. The announcement in ...
The updated requirements for post-market surveillance (PMS) under the EU Medical Device Regulation (MDR), EU In Vitro Diagnostics Regulation (IVDR), and the U.K.'s forthcoming Statutory Instrument (SI ...
The Ophir® SP920 USB 3.0 Silicon CCD High Resolution Beam Profiling Camera is designed to accurately capture and analyze wavelengths from 190 nm – 1100 nm, with enhanced sensitivity at 1070 nm. The ...
Unlocking the potential of RFID technology in the medical sector is crucial for optimizing operational efficiency and ensuring patient safety. This white paper highlights 15 reasons to embrace RFID ...
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