In fact, the FDA’s definition of a medical device ... won’t regulate multipurpose devices, like smartphones, just because they can run health-related apps. 3.Development processes for devices ...

The medical device industry can take steps right now on PFAS for safety, sustainability and to steer other industries in the ...

As drug developers rely increasingly ... biologics, and medical devices, and how they apply to medical research and development efforts at MRDC.

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective ... QMS problem remediation and FDA responses, new / changed product 510(k)s, process/ product/ equipment including QMS and ...

The spectrum of medical device products ranges widely in value, complexity and customization, from tongue depressors to CT ...

The U.S. Food and Drug Administration (FDA) recently announced it plans to phase out animal testing in the development of monoclonal ...

This approach attempts to strike a balance between innovation and oversight, but it's still an evolving process with ... The FDA regulates AI as a medical device under its Digital Health Software ...

ALBAWABA - The Food and Drug Administration (FDA), which is responsible for protecting public health by ensuring the safety, efficacy, and security of d ...