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

MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS Newswire / ...

From the founders of BoldType comes CyberMed, a new company dedicated exclusively to MedTech cybersecurity. With a mission to ...

The EMA anticipates that the ability to access scientific advice will foster innovation among medical device manufacturers.

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

As 2025 unfolds, the utility industry and its workforce stand at a unique crossroads, writes contributor Matthew Smith ...

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 ...

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

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

MDR Certification Strengthens Resyca's Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS Newswire / January 28, 2025 / Resyca BV, a pioneering leader in the development an ...