MedTech Predictions for 2021
We have the opportunity to refine processes that were implemented in a hurry during the pandemic, along with the insight to improve the entire healthcare system.
Tag Archives: Focus Article – Homepage
In 2020, FDA Authorized 132 Novel Medical Devices
The record-high number of authorizations last year was a significant jump over 2019.
How Hospitals and Health Systems Can Accelerate Innovation
Among the many lessons from the COVID-19 pandemic, it’s clear that the future of healthcare belongs to those who can harness science and technology—sometimes rapidly—to improve population health through more efficient and accessible care.
How Life Sciences Companies Can Level Up Healthcare Education in Post-COVID Era
It’s time for these companies to bridge the knowledge gap and transform how healthcare information is accessed and used.
Innovations in Self-Monitoring Blood Glucose Devices Will Impact Healthcare Services
Seamless and personalized diabetes care has become a new normal.
Five Best Practices to Grow MedTech Leadership Talent in Turbulent Times
In an industry fraught with constant challenges, medtech leaders need to close the growing skills gap of their employee base and develop leadership from within. The pandemic’s impact on an increasingly remote workforce has caused companies to adopt a new approach to cultivating emerging leaders.
Strategic National Stockpile Ventilators Can Support ‘Most’ Patients, but That Is Not Enough
Critical care hasn’t had many breakthroughs in recent years and in order to change that, I believe we need to put more of an emphasis on integrating technology—specifically artificial intelligence (AI) —into the field.
FDA Names Acting Director of Medical Device Cybersecurity
The agency created the new post within CDRH, effective January 1.
COVID-19 Introduces New Risks, Hazards in Health Tech
With the accelerated adoption of many new technologies, ECRI’s annual health technology hazards list has been transformed by the COVID-19 pandemic.
Regulatory Information Management Streamlines Processes and Supports Data Quality
Data integration is doing much to enhance regulatory information management. Life sciences companies are increasingly discovering useful interdependencies between data, documents and RIM processes. The next step is to put this data to work to improve efficiency.
