The Health Sector Coordinating Council’s Cybersecurity Working Group today released a best practices guide for health care organizations and medical device manufacturers that includes an updated ...
The new Propelus Prototype Centers in Oregon and Minnesota will help customers accelerate the pace of life-saving innovation.
The evolution of medical-grade thermoplastic polyurethanes (TPUs) continues to reshape possibilities for device manufacturers seeking materials that combine flexibility, durability and ...
The European Union has been a leader in recent years when it comes to regulatory reform intended to protect individuals’ privacy, safety, and health. As Europe leads the way, regulators in the United ...
ANSI/AAMI HE75:2025; Human factors engineering - Design of medical devices is the first update to AAMI's premier human factors standard since 2009. The standard is meant to assist users and ...
The Wearable Medical Devices Market is one of the fastest-growing segments within digital health, reflecting a powerful ...
In recent years, there has been a growing emphasis on sustainability across the healthcare industry, and the medical device manufacturing sector is no exception. As the world faces environmental ...
AI medical device companies face major reimbursement hurdles when trying to secure coverage, CPT codes, and payment from ...
Beyond Tariffs: The Software Supply Chain Risks Every Medical Device Manufacturer Should Be Watching
By reframing security as an investment rather than a cost, MDMs can reduce risk exposure, improve compliance readiness, and ...
Expertise from Forbes Councils members, operated under license. Opinions expressed are those of the author. Many medical device manufacturers are seeking alternatives to where their production takes ...
Key market opportunities lie in enhancing medical device QMS by addressing non-conformances and complying with ISO 13485 and 21 CFR 820 standards. This creates demand for training programs focused on ...
On June 19, 2025, the European Commission (“EU Commission”) adopted Regulation 2025/1197 imposing restrictive measures on Chinese medical devices in its first use of the European Union’s International ...
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