The "Best Practices for Supplier Qualification in Life Science Training Course (May 6th - May 7th, 2026)" has been added to ResearchAndMarkets.com's offering. Conduct thorough supplier qualifications ...

The next Medical Device User Fee Amendments, which will set how much the FDA can raise from the industry in fees over a ...

FDA commissioner Marty Makary revealed at the 2026 CES trade show in Las Vegas that low-risk devices will face less ...

Clinical expectations in minimally invasive interventions is rising, making collaboration in the medical value chain ...

Great Britain is entering a new era of MedTech regulation, with major pre-market changes expected that are designed to ...

Costa Rica hosts 100+ multinational medtech companies, attracting diverse medical device manufacturers and specialized ...

The U.S. Food and Drug Administration says it will ease regulatory requirements for certain consumer wearable health devices.

In June 2025, the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024 came ...

ProMed, a leading contract manufacturer specializing in medical-grade silicone and plastic components, provides comprehensive support for medical device, pharmaceutical, and combination drug-device ...

Anthropic has introduced Claude for Healthcare, a suite of artificial intelligence (AI)-based tools to assist healthcare ...

MDR, MDSAP, and FDA audits demand rigorous preparation, lifecycle traceability, and risk-based compliance for global market ...

Cybersecurity for industrial, semiconductor, and medical device cyber-physical products, focused on Taiwan compliance and ...