Ethylene Oxide (EO) sterilization is essential for medical device safety. Explore how Process Challenge Devices help validate ...

The core message of a new guidance issued by NHS England and MHRA is clear: ambient voice technology (AVT) tools that go ...

FDA warning letters highlight recurring patterns, systemic gaps, and evolving priorities that medical device manufacturers ...

Early recognition and mitigation of drug and device integration difficulties are critical to the success of combination ...

This article explains why Latin Americas demographic diversity, cost profile, and accelerating digital health infrastructure ...

This article describes how a mechanism-based risk analysis approach can provide two complementary opportunities for ...

This article describes the disadvantages of surgical sutures, advantages of surgical glues/sealants, and the properties of ...

New safety-certified MLCCs with up to 500 Vrms rating, compact design, and harsh-environment resilience deliver reliable high ...

As the medical device industry continues to expand, intellectual property (IP) considerations — especially those concerning patents — are critical for medical device innovators and ...

The FDA has issued its much-anticipated final guidance on cybersecurity risk management in medical devices, effective June 2025.

Artificial intelligence (AI) and machine learning (ML) are redefining healthcare, from enabling earlier diagnoses and personalized treatments to streamlining hospital operations and accelerating ...

The medical device sector faces significant changes, as both Donald Trump and Robert F. Kennedy Jr. have identified the FDA as a focal point for deregulation. What does this mean for medical device ...