Public Forum 2024 kicked off this week with experts from the National Evaluation System for health Technology (NEST), the ...

As laboratories navigate the evolving landscape of Laboratory Developed Tests (LDTs), the FDA’s phased approach to regulation ...

The value-based care model, with a substantial monetary budget, necessitates on-time and correct risk stratification. As a ...

HOUSTON – (Sept. 12, 2024) – Rice University and The University of Texas MD Anderson Cancer Center today announced the launch ...

Matter and HERIF announced the winner of the Inaugural Future HealthTech Leaders Innovation Challenge. Monarch Health, a digital behavioral health treatment program for children and adolescents with ...

Recently, biocompatibility consultant, MedTech enthusiast and chemist, Marina Daineko, shared a series of LinkedIn posts defining, medical device biocompatibility and the need for a Medical Device ...

To streamline processes, enhance transparency, and improve the overall efficiency of conducting clinical trials in the EU/EEA, the 3-year transition period from the CTD to the CTR requirements was ...

Changing market dynamics and the influx of data are driving the importance of building integrated data management infrastructures for MedTech companies to not only drive data integration, aggregation, ...

Fraudulent data is becoming more common by the submission. So much so that the FDA recently published a press release reminding medical device manufacturers to scrutinize Third-Party Generated Data.” ...