Articles tagged with “medical-devices”

Learn about ISO 13485:2016, the QMS standard for medical devices. Updated for 2026 with FDA QMSR effective date, EU MDR/EUDAMED timelines, AI/ML guidance, and certification data

Learn about the FDA's AI/ML medical device tracker. With 1,451 devices authorized through 2025 and 295 cleared in 2025 alone, we analyze authorization trends, specialty breakdown, foundation model milestones, and the evolving regulatory framework

Explore how Oracle Cloud CX supports customer experience in life sciences, encompassing CRM, marketing, and service applications for compliant engagement with HCPs and patients.

Learn how regulatory affairs ensures product compliance in health industries. Explore the fundamental role of AI and LLMs in modern regulatory processes, including the latest FDA/EMA joint guidance and EU AI Act requirements.

A comprehensive analysis of the remote patient monitoring landscape in the US healthcare system, examining technological advances, regulatory framework, and implementation challenges in 2025.

A comprehensive analysis of the life sciences job market in 2025, exploring emerging roles, skill requirements, salary trends, and career opportunities across pharmaceutical, biotechnology, and medical device sectors.

A comprehensive analysis of leading medical technology companies worldwide that are at the forefront of AI adoption, examining their innovative applications in medical imaging, diagnostics, robotic surgery, patient monitoring, and personalized medicine, with detailed profiles of each company's AI technologies and market impact.