Learn key principles of cleanroom design to support contamination control and meet GMP requirements in pharmaceutical manufacturing.

Then, in January 2024, the dormant fab was booted up again. Intel funneled billions into the facility, including $500 million ...

Intel funneled billions into the facility, including $500 million it was granted from the US CHIPS Act. Now, Fab 9 and its ...

Spray-coated carbon flower sensors on stretchable substrates detect six biomarkers at sub-nanomolar levels and distinguish ...

In this Pharma Matters Q&A, Amina Rahmoune of Nelson Labs evaluates and compares sterility testing in cleanrooms and isolators.

The effectiveness of air disinfection devices may now be measured in minutes, rather than hours, with a new technique from ...

ORCHARD PARK, NY, UNITED STATES, April 2, 2026 /EINPresswire.com/ -- Flow Safe, Inc., part of the Dresser Utility ...

FDA cites Medline Industries for quality violations in CAPA, cleanroom maintenance, and design verification, urging prompt ...

There has been hope for some time to get air taxis for civilian travel off the ground. Multiple companies are competing to bring this technology to the United States, and now the Federal Aviation ...

See how unified WES and TMS reduce labor and shipping costs, optimize parcel vs LTL decisions, and deliver faster ROI ...

The bustling halls of CHINAPLAS have once again become the epicenter of global industrial transformation, drawing thousands of professionals to witness the next generation of plastics and rubber ...