Its expansion is attributed to increasing regulatory requirements. The global preclinical medical device testing services ...

UK regulatory approval follows FemaSeed, FemVue and FemCerv clearance/approvals in the U.S., Europe, Canada and Israel.

Several executive orders recently signed by US President Donald Trump may have significant implications for the US Food and Drug Administration ...

The debate over tighter regulations for electric scooters has intensified after new data revealed a significant number of ...

The EU MDR certification is recognized globally for ensuring that medical devices meet stringent requirements ... and compliance with the highest regulatory standards. Signifier is a pioneer ...

Signifier Medical Technologies Limited (“Signifier”), a global leader in medical technology for sleep-disordered breathing, announces that it has achieved the EU MDR certification for eXciteOSA ®, its ...

As AI in the medical device space rises, it likely means 2025 will be another challenging year for cyber threats in healthcare.

Medical devices comprise electronic equipment, implants, consumables and disposables, surgical instruments and in-vitro ...

With MDR certification, Resyca is strategically positioned to support its pharmaceutical partners in navigating the complex European regulatory landscape for Medical Devices and Drug-Device ...