AI server racks now exceed 100 kW, reshaping datacenter power design. Learn how evolving capacitor technologies enable stable, efficient power conversion in next-generation AI infrastructure.

As routine labs, imaging, and information from wearables and the environment stream in, a digital twin can model trajectories and suggest next actions, turning diagnostics into a living operating ...

Manufacturers must cut decision delays, harness AI to unlock messy data, embrace adaptive automation, and empower teams to act as force multipliers. See how these shifts define the path to resilience.

AI is reshaping quality in life sciences, but many teams struggle to balance innovation with audit readiness. Learn how industry leaders are managing risk and building confidence with AI.

While Mexico's health authority, COFEPRIS, has streamlined registration for medical devices, a dangerous shadow regulation has emerged with ad hoc stringent cybersecurity requirements. Stability ...

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

The digital revolution that resulted in the Internet of Things (IoT), Internet of Medical Things (IoMT), Software as a Medical Device (SaMD), and connected devices permeating the healthcare ...

The U.S. Food and Drug Administration (FDA) has issued its much-anticipated final guidance on cybersecurity risk management in medical devices, effective June 2025. This document, titled ...

In 2023, the FDA made the electronic Submission Template And Resource (eSTAR) mandatory for most 510(k) submissions. Although eSTAR is not an AI tool, the move was the first definitive leap toward the ...

SCS devices deliver electrical pulses to the spinal cord to relieve chronic pain. They are often used as treatment for failed back surgery syndrome, injuries to the spinal cord, complex regional pain ...

AI-assisted symptom recognition and pattern matching leverages machine learning to analyze vast amounts of medical data, including patient histories, clinical notes, and research publications, to ...

Regulation (EU) 2017/745 Medical Device (EU MDR) of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002, and ...