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Viable Particle Counting Articles & Analysis
9 articles found
In today’s world, precision and cleanliness are critical in industries like pharmaceuticals and biotechnology. Among the many tools used to maintain strict cleanliness standards, viable air samplers stand out as a key player. But why are these devices so essential? Let’s dive into the ...
Is there an international standard or guideline for sampling 1m³ total particle counts and viable particles with air samplers like the MiniCapt® mobile device for routine monitoring of production areas with classifications A, B, C, and D? ...
Cleanroom particle counting is essential for accurate functioning and meeting certification criteria in controlled environments. In this blog post, we take a look at five key principles of cleanroom particle counting, exploring the significance of each principle and how it contributes to maintaining the safety and quality of products manufactured in such ...
Question: “What is the need of taking a non-viable particle count after a power shut down for an hour. Our Class C area is stabilizing after 30 minutes of a power ...
The MiniCapt Mobile microbial contamination monitoring instrument now helps you further reduce contamination introduced during monitoring activities with a new antibacterial housing. Did you know that Particle Measuring Systems recently released the MiniCapt Mobile Microbial Particle Counter with a new antibacterial housing? In an effort to mitigate the introduction of bacterial contamination ...
Viable, non viable particle counts: Environmental and Process Monitoring- Annex 1, Section 9.4 In Part 3 of our 5 part blog series, we look at Viable Non Viable (V/NV ) Particle counts regarding Environmental and Process Monitoring as found in Annex 1, Section ...
The first table below controls for non viable particulate in the clean environment, including compressed gases. ...
The type of contamination being monitoring is either total particle (non-viable) or viable. Requirements for All Types of Monitoring The locations, frequency, volume, and duration of monitoring should be determined based on the risk assessment and the results obtained during the qualification. ...
Abstract For aseptic manufacture of pharmaceutical products there has been a shift in procedures for particle measurement, primarily due to legislative regulations. Traditionally, monitoring has been the classic portable monitoring of a cleanroom. ...