Cyberattacks and data theft are a serious problem in many industries, but in healthcare the consequences could be physically dangerous or even deadly or enrich the pockets of bad actors on the dark ...

ANSI/AAMI HE75:2025; Human factors engineering - Design of medical devices is the first update to AAMI's premier human factors standard since 2009. The standard is meant to assist users and ...

On December 29, 2022, President Biden signed a new statute that will significantly impact medical device cybersecurity regulation. Section 3305 of the Consolidated Appropriations Act of 2023 (“Section ...

New Delhi: India is set to overhaul standards for medical devices, strengthening the regulatory framework for the country's $12-billion market and aligning with US, Japanese, and European Union (EU) ...

While healthcare policy efforts have focused on data sharing between electronic health record systems, they have overlooked fragmented data in medical devices, contend researchers, who want to see an ...

The European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry (COCIR) issued a position paper on Tuesday to facilitate the harmonization of medical device ...

The FDA has received multiple reports of patients who have required medical attention, including hospitalization, after self-medicating with ivermectin intended for livestock. Source - U.S. Food and ...

There’s a growing movement among medical device manufacturers to develop industrywide cybersecurity standards that offer flexibility to innovate while providing basic protections against the emerging ...

MES software is transforming medical plastics manufacturing by automating compliance and enabling real-time traceability.

Medical software is the backbone of modern healthcare, supporting electronic health records (EHRs), diagnostic systems, imaging technologies and embedded software in medical devices like pacemakers ...