Wrapping up Q3 earnings, we look at the numbers and key takeaways for the medical devices & supplies - imaging, diagnostics ...

It’s time to remove Chinese medical devices from U.S. hospitals and close the data backdoor, because patient privacy and ...

The FDA said it plans to accept new forms of real-world evidence in product applications, starting with a subset of medical ...

Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...

FDA loosens data rules for medical devices by allowing real-world evidence without patient identifiers in marketing submissions.

Medical devices are Costa Rica's top export in 2025, overtaking knowledge-intensive services after a decade of growth by the medical tech industry.

Since the 2017 publication of the medical device regulation (MDR) and the IVD regulation (IVDR), EU regulations for medical ...

The FDA announced that it removed a limitation on the use of real-world evidence (RWE) in drug and device application reviews ...

The Illinois lawmakers want an electronic format for medical device makers to quickly and transparently report recall ...

Access to autism evaluations through specialty health care is notorious for long wait times across the United States. In ...

If finalized, the changes would reduce the scope of AI regulations for medical devices and include more provisions for rare ...