Environmental Monitoring
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Customizable Solutions For Cleanroom Facility Monitoring
10/31/2021
In pharmaceutical environments, “facility monitoring” or “environmental monitoring” refer to systems that help pharmaceutical​ manufacturers monitor and control the viable and non viable contamination in their cleanrooms​. This includes managing data from particle counters, microbial samplers, temperature/humidity sensors and more. In this conversation, Daniele Pandolfi and Blu Buquoy discuss Facility Pro products that are offered by Particle Measuring Systems. ​
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Real-Time Information On Microbial Contamination In Pharma Cleanrooms
4/25/2014
Watch to learn about the BIOTRAK® Real-Time Viable Pharmaceutical Particle Counter from TSI, which provides real-time information on microbiological contamination in pharmaceutical cleanrooms.
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Reduce Production Waste In Pharmaceutical Manufacturing
7/20/2022
Learn how cleanroom technicians can perform confident, reliable aseptic microbial monitoring in pharmaceutical manufacturing Grade A and B environments with external vacuum systems.
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Cleanroom Manufacturer Expands Capacity To Meet Industry Needs
12/12/2019
AES Clean Technology builds more cleanrooms than anyone else. The market is busy, and so are we... but are we too busy? The answer is a resounding "NO, AES is not too busy!" We plan our cleanroom design, panel manufacturing, and manpower loading and scale as needed. We currently have the capacity to more than double our panel manufacturing.
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Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing
1/4/2021
The Faciliflex Module is a transformational new concept in designing cleanrooms for the production of lifesaving therapeutics.
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Considerations & Steps For Building A Contamination Control Strategy (CCS)
9/30/2021
Defining a Contamination Control Strategy (CCS) is unique for each process and requires an intimate understanding of both the process and how to implement an effective strategy.
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The Evolution Of Pharmaceutical Modular Cleanroom Technologies And Project Execution
10/22/2020
AES Clean Technology is expediting the delivery of fully functioning cleanrooms. Modular technology allows for repeatable installations of proven systems. New facility projects are time consuming and have thousands of decision points. AES has simplified this process offering standardization. The three models AES offers have taken into consideration the trends seen with modern facilities offering built-in flexibility. AES is also capable of working collaboratively with clients to design–build high-quality customized cleanroom systems with guaranteed performance.
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Water Activity Is A Critical Parameter For Microbial Stability
10/26/2022
Learn about USP <1112> Application of Water Activity Determination to Non-sterile Pharmaceutical Products and USP <922> Water Activity, and why water activity is a critical parameter for microbial stability.
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Single-Use Active Air Microbial Monitor Guidance
4/20/2022
In this video, we demonstrate how to tell the BioCapt Single-Use (BCSU) 25/50 LPM from the 100 LPM plates, what their individual applications are, and which active air sources are applicable for use.
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ISO EN 17141 And ISO 14698 Overview
3/3/2022
Gain insight into the standard for microbiological monitoring and control, ISO/EN 17141, and how it harmonizes with ISO 14698 parts one and two.