Why are Some Microbiology Media Autoclaved While Others are Irradiated?
This article explores how sterilization methods are selected for prepared microbiology media: Why...
Managing BSE/TSE Risk in Prepared Microbiology Media: What You Need to Know
In this article we’ll cover: Why BSE/TSE remains a concern for users of prepared microbiology...
Evaluating and Validating Potential New Suppliers of Prepared Microbiology Media
Selecting a new supplier of prepared microbiology media is a significant decision in pharmaceutical...
Building a Robust Contamination Control Strategy with Redipor® TwistLock: AnalytiChem UK Featured in Cleanroom Technology
Exploring how Redipor TwistLock culture media plates from AnalytiChem UK strengthen cleanroom...
Annex 1 and GMP: Key Differences Across Manufacturing Scales in Sterile Drug Production
Overview Annex 1 of the EU Guidelines for Good Manufacturing Practice (GMP) provides a unified...
Environmental Monitoring Plates: Things to Consider
Effective environmental monitoring is essential for contamination control in regulated industries....
Common Challenges and Considerations in the Processing of Microbiology Tests in the Food Industry
Microbiological testing plays a critical role in ensuring food safety. Regulatory bodies such as...
What Causes Condensation in Agar Plates?
Condensation in agar plates is a common issue, but what causes it, and how can it impact...
Agar Plate Desiccation: Cherwell's Insights Feature in Cleanroom Technology
Desiccation of agar is a significant challenge in pharmaceutical environmental monitoring (EM). It...