Key market opportunities include enhancing regulatory compliance for medical devices through process validation. Understanding quality management ties, FDA/EU/UK guidelines, and GAMP standards grants ...

How integrated pharmaceutical manufacturing helps CDMOs simplify scale-up, reduce complexity, and move from raw materials to finished dosage forms faster.

The industry is buzzing about AI agents that could automate this work. But here’s what most companies miss: You can’t hand ...

Medical physicist Todd McNutt explains how Plan AI, an artificial intelligence-powered plan quality software solution, uses ...

Is your medical device company ready for the QMSR shift? Engineer Aldo Vidinha explains why "checkbox compliance" is over and how the FDA’s alignment with ISO 13485 redefines quality as a connected, ...

CX platforms process billions of interactions yearly — but no security tool monitors what their AI engines ingest. Six blind ...

This issue of the journal features a Series of three papers on artificial intelligence (AI) in infectious diseases. The Series, led by Anna Odone (University of Pavia, Italy) and published online in ...

Digital transformation has, for most modern manufacturers, become a survival requirement. Yet despite investing in tablets, apps, and dashboards, many factories still struggle with the same ...

A new third-party certification program establishes requirements for HIPAA, 42 CFR Part 2, clinical quality, patient ...

Cloud seeding programs are now taking place in more than 50 countries across the globe, according to the World Meteorological Organization.

Bringing AI agents and multi-modal analysis to SAST dramatically reduces the false positives that plague traditional SAST and rules-based SAST tools.