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...
Strengthening Global Pharmaceutical Standards: WHO’s 10th Edition of Quality Assurance Compendium
Overview In February 2024, the World Health Organization (WHO) released the 10th edition of its...
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...
Cleanroom Compliance on the Move: AnalytiChem’s UK Site Featured in Cleanroom Technology Magazine
Exploring the power of portable air sampling in meeting modern regulatory expectations
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...