NewsClose-up of viable microbial bacteria colonies for contamination monitoring.

Viable Air Sampling

Introduction to Viable Air Sampling: Viable Environmental Monitoring Regulations related to viable air sampling play a pivotal role in shaping contamination control strategies in pharmaceutical manufacturing. The dynamic interplay of these regulations, both direct and indirect, is crucial for ensuring the safety and efficacy of drug products. With the advent of modern manufacturing concepts and the evolution of industry standards, the adoption of viable air monitoring becomes imperative to align with the latest regulatory trends.

NewsContinuous Monitoring Concept

FAQ’s: Class D Particle Monitoring Requirements

Question:Ā ā€œCan you speak to the requirements for monitoring Class D clean areas for viable and nonviable particulate. The regulations don’t make it black and white.ā€

NewsAnnex 1 compliant continuous microbial monitoring solution EU GMP Annex 1

EU GMP Annex 1 – Commonly Asked Questions

Welcome to ourĀ EU GMP Annex 1Ā questions and answers blog, where experts answers commonly asked questions about the latest changes to regulation.

NewsGranite surface plate used as a precision reference base for inspection and measurement.

BLOG: GPT Anaerobic Cultures

What Is GPT? The Growth Promotion Test (GPT) determines the appropriateness of the culture media to be used in environmental monitoring sampling. The medium is challenged with a small number of microorganisms to assure the nutritive properties, functionality and media quality are adequate for the detection and enumeration of microbial…

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