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environmental monitoring regulations
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.

Isokinetic Sampling

In the highly regulated and risk-sensitive world of pharmaceutical manufacturing, adherence to stringent compliance measures is paramount. To achieve this, pharmaceutical companies use controlled environments, particularly cleanrooms, where the risk of variability and particle contamination is minimized. Here we’ll delve into the significance of cleanrooms and explore a key contamination management technique employed within them—Isokinetic Sampling and unidirectional airflow.

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