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NewsPMS Particle Counter Calibration and Service

Protect Clean Manufacturing with Regular Particle Counter Calibration

NewsGMP cleanroom contamination monitoring

10 Tips to Safeguard Your Cleanroom Through Proactive Contamination Monitoring

   

Cleanroom Standards, Classification and Compliance – Quick-Reference Guide

Particle Measuring Systems has created these Cleanroom Standards, Compliance & Classification quick-reference cards. A free quick-reference tool designed to help you navigate cleanroom standards with ease.

Newscompressed gas monitoring compressed gas compressed gas systems

Compressed Gas Systems in Aseptic Manufacturing

Discover the importance of compressed gas risk assessment in pharmaceutical manufacturing. Learn how to ensure product quality and compliance through effective management of compressed gas systems, including their design, operation, and monitoring.

Newscompressed gas monitoring compressed gas compressed gas systems

Compressed Gas Contamination: Guidelines for Control in Aseptic Manufacturing

Ensure the integrity of your manufacturing processes with our comprehensive guide on maintaining the cleanliness of compressed air systems. Discover essential guidelines for identifying contaminants, monitoring practices, and preventive maintenance strategies to meet regulatory standards. Learn how Particle Measuring Systems can support you in achieving optimal air purity and safeguarding product quality.

Newsactive air sampling

Optimizing Microbial Air Sampling to Reduce False Positives in Cleanrooms

In this blog, we’ll explore how modern innovations, like the BioCaptĀ® Single-Use microbial impactor, can enhance microbial air sampling efficiency while reducing the risk of false positives in cleanrooms.

NewsMedia Dehydration and Biological Recovery Efficiency

Microbial Sampling Criteria

In the pharmaceutical manufacturing industry, ensuring sterility and minimizing microbial contamination are critical for maintaining product quality and safety. Microbial sampling is a key component of environmental monitoring, and understanding the optimal criteria for sampling can significantly impact the effectiveness of sterility assurance programs. Learn about optimal microbial sampling criteria here.

NewsCleanroom Classification Contamination Control Strategies

Contamination Control Strategies for Innovation FAQ’s

In the pharmaceutical industry, maintaining stringent contamination control is not just a regulatory obligation but a fundamental aspect of ensuring product safety and efficacy. The EU GMP Annex 1 outlines the importance of a Contamination Control Strategy (CCS) for sterile drug products, emphasizing the need for a structured approach to manage risks and maintain compliance. We recently hosted a webinar discussing these strategies in detail. To help navigate this complex field, we’ve compiled a list of frequently asked questions from our experts.

NewsISO Registrations

IT Outages and Continuous Cleanroom Monitoring During with FacilityProĀ®

Our Facility ProĀ® environmental monitoring system showcases exceptional performance during internet outage events, ensuring uninterrupted and continuous cleanroom monitoring and control. Facility Pro is a vital component of our Facility Monitoring Systems (FMS) product line, integrating sampling, reporting, and data retention of particle, microbial, and environmental data.

NewsApplying Appropriate Limits in Cleanroom Monitoring

Applying Appropriate Limits in Cleanroom Monitoring

Protect the cleanliness of your environment by utilizing limits in cleanroom monitoring, including standards like ISO 14644-1:2015 and the EU GMP Annex.

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