FDA warning letter data reveals the same top 10 compliance issues have plagued medtech for 20 years, with CAPAs leading at 12 ...

ClariMed experts reveal how gender bias in medtech leads to safety risks for women and share strategies to create more ...

On February 2, 2026, the U.S. Food and Drug Administration (FDA) published its anticipated compliance program manual, ...

MedTech manufacturers are pushing for greater precision. Nordson EFD, a fluid dispensing systems specialist, is optimizing with automated and jetting systems. Integrated MES, ...

Regal Rexnord discusses core brake components and specifications that support compact, mobile and safety‑critical ...

Redefining hydrophilic coatings solutions by uniting advanced chemistry, device engineering and customer-first ...

An integrated mechanical brake, for which Schaeffler has filed a patent, forms a central part of the actuator’s safety concept. When the motor is de-energized, the brake securely holds the actuator – ...

New capability delivers end-to-end traceability across all product development data, connecting milestones, decisions, and evidence across every phase of the medical device lifecycle.

Has CDSCO Guidance Changed The Rules? Legal News and Analysis - India - Regulatory & Compliance - Conventus Law ...

Dave Evans argues that North America’s next manufacturing boom will be defined by speed, resilience, and systems built for ...

Key Takeaways - FDA’s 2026 guidance clarifies when digital health tools fall outside device regulation. Updated policies for clinical decision ...