Should Hospital Pharmacies Review Their Environmental Monitoring Programs Under EU GMP Annex 1?
Why patient risk — not production scale — sets the compliance bar
What Does EU GMP Annex 1 Require for Continuous Environmental Monitoring?
Why continuous monitoring is a risk control mechanism, not a sampling exercise
Single-Vent vs. Triple-Vent Microbiology Media Plates: What’s the Difference?
This article explores how single-vent and triple-vent microbiology media plates differ, and how...
Desiccation in Agar Plates: Causes and Prevention
This article covers desiccation of agar in environmental monitoring plates. We'll explain why it...
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...