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
05Sep
Kinetic vs Gel Clot Method in BET Testing: Which One Do You Need?
If you work in the pharmaceutical or medical device industry, you’ve probably heard someone say, “We’ve done BET testing.” It
05Sep
MAT vs BET: Why the Monocyte Activation Test Is the Safer Choice for Pyrogen Testing
If the Bacterial Endotoxin Test (BET) can detect endotoxins at concentrations as low as 0.005 EU/mL, why are regulators and
31Jan
A Comparative Analysis of Disinfectant Efficacy Testing Methods: Which One Is Best for Your Industry?
In industries where cleanliness is a top priority—such as pharmaceutical, medical device manufacturing, food processing, and healthcare—disinfectant efficacy testing is