CISA updates software bill of materials guidance to clarify SBOM requirements for medical device makers under FDA rules effective Oct. 1, 2023.

The Cybersecurity and Infrastructure Security Agency and other U.S. and international agencies July 29 released joint ...

High-level turnover has introduced uncertainty about how quickly the FDA’s agency-wide AI strategy will move forward.

Throne Science, an Austin startup whose AI-powered toilet camera launched to consumers just four months ago, has closed a $10 million Series A round — funding the one health-monitoring category that ...

A key theme emerging from FDA complete response letters since 2018 is that data system validation is lacking in the ...

As a Java Software Engineer, you will work on software that truly makes a difference. You will develop robust applications that support researchers, analysts, and Defence personnel in tackling complex ...

Stroke patients who arrive at a hospital with a large blood clot blocking a major brain artery now have a new treatment ...

Patent attorney Jay Halt explains how medtech companies should align IP strategy with FDA compliance to avoid unenforceable patents and regulatory issues.

Dynamic AI systems applied in biopharmaceutical manufacturing must be governed within established regulatory frameworks.

Background/Aims Retinopathy of prematurity (ROP) zone classification guides disease severity assessment and Early Treatment ...

This voice experience is generated by AI. Learn more. This voice experience is generated by AI. Learn more. Over the last several years, I've worked with engineering teams building software for life ...

The life sciences industry has always operated under pressure to stay ahead of regulatory change. But 2026 has raised the stakes considerably, bringing not just one significant shift, but several that ...