Medical device design and development is a process that helps to ensure devices that go to market are safe, effective, marketable, and profitable. The process is a blueprint of the phases needed to ...

Small medtech companies can leverage AI without huge investments to compete with major manufacturers using targeted approaches.

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...

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

Discover how software developers for medical-device OEMs are balancing innovation and safety, and the challenges they face in making it happen. The medical-device industry is rapidly advancing, from ...

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.

With Covid accelerating time-to-market for medical devices, digital tools play a key role in managing converging priorities for device manufacturers.

Saideep Nakka is a principal systems engineer specializing in medical device innovation, with over 9 years of industry experience. His educational background includes a Master’s in Engineering ...