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Digital Health


Medtech, innovation
January 15, 2021
Medtech, innovation

FDA: COVID-19 Put Spotlight on Digitization of Healthcare, and Importance of Data, Communication and Collaboration

By Maria Fontanazza

During this week’s Consumer Electronics Show, FDA Principal Deputy Commissioner Amy Abernathy talks about lessons learned from the pandemic and 2021 goals.

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Jonathan Wiesen, MediOrbus
January 13, 2021
Jonathan Wiesen, MediOrbus
Soapbox

Future of Specialty Telemedicine

By Jonathan Wiesen, M.D.

Its success lies in a synergy between the technological and the clinical.

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Roger Sands, Wyebot
January 8, 2021
Roger Sands, Wyebot
MEDdesign

Preparing Your WiFi Network for the Future (Part 2)

By Roger Sands

How artificial intelligence and automation play an important role in future-proofing networks.

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Roger Sands, Wyebot
December 31, 2020
Roger Sands, Wyebot
MEDdesign

Preparing Your WiFi Network for the Future (Part I)

By Roger Sands

The wireless network serves as the backbone supporting patient care in every department of a healthcare facility. It is crucial to optimize and future-proof WiFi networks.

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magnifying glass
December 23, 2020
magnifying glass

In 2021 Predictions, Digital Health Reigns Supreme

By Maria Fontanazza

Leveraging the power of technology to create a more patient-centric approach and consolidate costs is expected to play a big role.

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Oliver Schacht, Ph.D., OpGen
December 22, 2020
Oliver Schacht, Ph.D., OpGen
Soapbox

Cloud-Based Informatics Enable Smarter Antibiotic Use and Infection Control

By Oliver Schacht, Ph.D.

Incorporating bioinformatics platforms can ease the burden of tracking, analyzing and managing the use of antibiotics.

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Shady Hassan, Vocalis Health
December 9, 2020
Shady Hassan, Vocalis Health
MEDdesign

Returning to ‘Normal’: Non-Invasive Screening Via Vocal Analysis

By Shady Hassan, M.D.

A return to normalcy requires us to address the limits of current testing approaches and broadly deploy reliable screening tools that facilitate early detection and encourage more focused testing of those at high-risk of spreading the coronavirus.

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Columns

August 20, 2026

AI-Assisted Triage: Accelerating Post-Market Surveillance While Eliminating Reporting Blind Spots

By Binitkumar M. Vaghani

Complaint volumes have outgrown manual triage, and medical device companies are turning to AI to keep up. The speed gains are real, but used carelessly the same tools can bury a reportable event at the bottom of a queue while the MDR clock runs. This piece maps where AI genuinely helps in post-market surveillance, where human judgment has to stay, and what validation, monitoring, and audit trails a defensible program needs. It is grounded in the current regulatory frame, including the QMSR and FDA's new inspection program (CP 7382.850) that took effect February 2, 2026, 21 CFR Part 803 reporting timelines, and ISO 13485 software validation expectations. It includes a practical table drawing the line between tasks that are safe to automate and decisions that must stay human-owned. The intended audience is quality, regulatory, and post-market surveillance professionals in the medical device industry.

August 19, 2026

Sensors at the Edge: Powering Smarter Healthcare

By Daraius Patell

As healthcare shifts towards remote monitoring, connected devices and decentralized care, sensor technologies are becoming increasingly foundational to how medical devices collect, validate and transmit critical information. From remote patient monitoring and at-home care to connected medical devices and robotic-assisted surgery, sensing technologies can help enable earlier detection, more reliable clinical data and better-informed decision making.

August 18, 2026

FDA Seeks Public Feedback to Inform Regulatory Approach for Generative AI-Enabled Medical Devices

GenAI-enabled medical devices hold transformative promise for patient care and the broader health ecosystem. At the same time, these devices may introduce unique risks when compared to traditional software and AI-enabled medical devices.  

August 6, 2026

The Interface is the Risk: A MedTech Blueprint for AI and System Integration

By Aneesh Deshpande

Catastrophic failures rarely stem from isolated hardware bugs. They breed where hardware, firmware, wireless telemetry, and clinical workflows intersect. These silent data integrity failures can invalidate entire research efforts without real-time detection, squeezing V&V Engineers between exploding complexity and compressed timelines.

August 3, 2026

Beyond the Status Report: Using LLMs to Reveal the True State of SaMD Development

By Shreya Sridhar
SaMD Readiness

Medical device software development teams have always struggled with a deceptively simple question: How much of the system is actually complete?

July 8, 2026

Zimmer Biomet to Hire 500 in India as New Bengaluru Technology Centre Drives AI and MedTech Innovation

By MedTech Intelligence Staff
ZimmerBiomet

Zimmer Biomet will hire 500 professionals over the next three years for its new Bengaluru technology centre, expanding its AI, software engineering, and R&D capabilities as India strengthens its position as a global healthcare innovation hub.

July 8, 2026

AdaptHealth Investigates Data Breach After Social Engineering Attack, Possible Link to ShinyHunters Emerges

By MedTech Intelligence Staff
AdaptHealth

AdaptHealth is investigating a material cyberattack after attackers used a social engineering scheme to compromise a third-party contractor's account, stealing patient data from its cloud-based systems as reports link the breach to the ShinyHunters extortion group, though the attribution remains unconfirmed.

July 7, 2026

Applying Agentic AI to Healthcare Delivery: The Key to True Transformation

By Jaimon Jose
AI in the EHR

MTI Viewpoints Insights shared by industry relative to healthcare and the advancement of medical technology. Jaimon Jose, senior director of engineering and compliance at CharmHealth, is a software architect and technical leader with more than 18 years of product development...

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