Pathogen Testing in Purified Water: Why Pharma Tests Beyond USP, EP and JP
If you have worked with Purified Water (PW) in pharmaceutical or medical device manufacturing, you may have asked a fair
11Oct
09Oct
Hydrogen Peroxide vs Formaldehyde Fumigation in Cleanrooms: Why Pharma Is Making the Switch
For years, many pharmaceutical facilities treated formaldehyde as the “perfect” fumigant. It was cheap, it killed microbes, and it appeared
04Oct
Feller Correction in Air Sampling: Why r and Pr Start Differing
During a routine air sampling check, a simple question came up: “Why do r and Pr start differing after 17?”
03Oct
Settle Plate Placement in Cleanroom: Why Location Decides Everything
Picture an aseptic cleanroom on a good day. The HEPA filters are performing efficiently, differential pressures are within limits, and
27Sep
Environmental Monitoring Trending in Pharmaceutical Manufacturing: Why One Isolate Is Never Just One Isolate
Is your environmental monitoring (EM) program actually strengthening your contamination control strategy or is it just generating paperwork that gets
02Feb
Mastering Bacterial Endotoxin Testing: A Comprehensive Guide for the Pharmaceutical Industry
Bacterial endotoxin testing (BET) is an essential component of quality control in the pharmaceutical and medical device industries. Endotoxins, toxic