Engineers could avoid expensive redesigns by planning medical device testing early in development with expert guidance.

Regulated healthcare companies are under increasing pressure to move faster while maintaining the highest standards of ...

Cambridge, UK - Regulatory compliance in medical device development is often treated as a hurdle to be cleared late in a ...

Look out for practical AI capability and next-generation materials at this year’s MD&M West 2026, says Alleima ...

At MD&M West 2026, Carl Douglass cuts through the hype to show how additive manufacturing truly accelerates Class II and III ...

The Atomic Spectroscopy Group at the National Institute of Standards and Technology, which provides definitive measurements integral to developing biomedical instrumentation that helps diagnose health ...

Many medical device companies develop software using a traditional waterfall methodology in which each step is taken in sequence: requirements, design, implementation, verification, and validation ...

A rendering of Aggie Square, the UC Davis science, innovation and learning hub in Sacramento. The UC Davis Department of Biomedical Engineering is launching a new nine-month master’s degree program in ...

Genesis Innovation Group, a medical device development firm, has formed Capitan Orthopedics, a new subsidiary branch, ...

The advent of artificial intelligence (AI) and data-driven methodologies has triggered a wave of transformation in regulatory compliance and quality assurance for the development of medical devices.

WEST CHESTER, Pa.--(BUSINESS WIRE)--Archimedic, a medical device development firm that provides Design, Regulatory, and Go-to-Market services to its clients, has launched OpenQMS, an open-access, ...

Assessing the chemical makeup of a medical device as part of the safety evaluation can either be a blessing for manufacturers by shortening the time to market or entail some surprises, according to ...