This training unlocks opportunities for companies to modernize GxP validation by shifting to Computer Software Assurance, ensuring data integrity and compliance with FDA regulations, and addressing ...

The FDA will ease regulation of digital health products, aiming to deregulate AI and promote its widespread use.

BrainSpace announced that the FDA granted 510(k) clearance for its Intellidrop automated brain fluid management system.

Here are 40 spine devices and technologies earning FDA clearances in 2025. Note: This is not an exhaustive list. 1. SurGenTec earned FDA 510(k) clearance for its OsteoFlo HydroFiber to be used as a ...