Understand cGMP requirements for portable environmental monitoring to support contamination control in pharmaceutical cleanrooms.

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

Biopharmaceutical manufacturing relies on many advanced technologies. Still, many pharma companies have room to improve when it comes to taking full advantage of everything modern tech has to offer.

WILMINGTON, Del., April 8, 2026 /PRNewswire/ -- LabWare, a global provider of laboratory informatics, and Phizzle, an innovator in laboratory data integration, today announced a partnership to ...

JCB Laboratories, a sterile compounding pharmacy in Wichita, Kan., has installed a continuous cleanroom monitoring system from Fremont, Calif.-based Lighthouse Worldwide Solutions to help catch ...

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

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At the forefront of medical innovations, medical device manufacturers have undergone a remarkable transformation in recent years, driven by technological advancements and heightened demands for ...

TOFWERK is a profitable innovator in compact, ultra-fast time-of-flight (TOF) mass spectrometry for real-time air and semiconductor cleanroom monitoring, food, flavors & fragrances markets, and ...