ENVIRONMENTAL MONITORING
Particle Measuring Systems' FMS Solution At Argonaut Manufacturing Services
When Argonaut Manufacturing was setting up their new state-of-the-art fill line (a VarioSys line by Bausch & Stroebel and SKAN), they wanted the best contamination monitoring solution to ensure proven product reliability for their customers. The problem was, they had ...
Get Your Aseptic Facility Ready For EU GMP Annex 1
Here, we review contamination control strategy (CCS) considerations, the setup of a microbiological environmental monitoring program, and how to optimize the design of hardware and consumables for specific environments.
A Real-Time Viable Particle Counter To Identify Contamination Source
Here, we introduce a real-time viable particle monitor and how it can quickly identify the source of contamination in pharmaceutical cleanrooms.
The Evolution Of Pharmaceutical Modular Cleanroom Technologies And Project Execution
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 offer...
Water Activity Is A Critical Parameter For Microbial Stability
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.
Compressed Gas Risk Assessment: A Significant Step In Your CCS
Discover the importance of compressed gas monitoring in ensuring product quality and compliance with EU GMP standards.
Real-Time Information On Microbial Contamination In Pharma Cleanrooms
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.
Cleanroom Manufacturer Expands Capacity To Meet Industry Needs
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 nee...
USP<1788>2022 Revision Summary
Review the latest revisions to the USP<1788>, which has expanded to support a holistic view of finished product contaminants, how they should be investigated, and added flow imaging technologies.
AES Clean Technology Career Opportunities
AES Clean Technology provides industry-leading modular clean room facilities with career opportunities in design, manufacturing, installation and sales. Hear how our current employees came on board to AES and what they enjoy about their careers.
Single-Use Active Air Microbial Monitor Guidance
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.
How Crucial Is Culture Media Selection In Environmental Monitoring?
Explore culture media regulatory requirements, the impact of manufacturing guidelines and media features and specifications on environmental monitoring, and the importance of media supplier selection.
Safety Department At Cleanroom Manufacturer Ensures No One Gets Hurt
AES takes the well-being and safety of all of our team members very seriously. In this video, AES director of EHS Tony Mangabat highlights some of the measures our safety department takes to ensure no one gets hurt at AES.
Understanding ISO 21501-4 – Particle Counter Calibration
In this webinar we review how to be compliant with the most recent particle counter calibration requirements, particle counter terminology, and how a particle counter works in theory.
Annex 1 Ready Cleanroom Classification Testing
Discover a portable particle counter that ensures your classification testing complies with the revised EU GMP Annex 1 with updated limits and the ability to define limits that are no longer specified.
Airflow Visualization Studies: The Impact Of Annex 1 On Sterility Assurance
Airflow visualization techniques like Smoke Studies and CFD analyses are crucial for contamination control, aiding cleanroom qualification, environmental monitoring, and optimizing contamination control strategies under Annex 1.
Reduce Production Waste In Pharmaceutical Manufacturing
Learn how cleanroom technicians can perform confident, reliable aseptic microbial monitoring in pharmaceutical manufacturing Grade A and B environments with external vacuum systems.
Faciliflex Cleanroom Module For Therapeutic Drug Manufacturing
The Faciliflex Module is a transformational new concept in designing cleanrooms for the production of lifesaving therapeutics.
The Successful Implementation Of A New Aseptic Filling Line
Discover how a Quality by Design approach can streamline the development of new sterile product filling lines, featuring a real-life example illustrating its effectiveness.
Deliver Contamination Control Solutions To An AUSTAR Customer
In this video interview, the team from AUSTAR UK discuss why and how they worked with Particle Measuring Systems’ (PMS) exclusive UK distributor, EMS Particle Solutions, to provide an AUSTAR Sterility Test Isolator customer with a complete viable and non viable cont...
Scope 3 Emissions: Cut The Complexity With Creative Collaboration
Delve into the crucial role of Scope 3 emissions in the biopharma industry's sustainability journey, and learn more about the challenges and opportunities of managing these types of emissions.
ISO EN 17141 And ISO 14698 Overview
Gain insight into the standard for microbiological monitoring and control, ISO/EN 17141, and how it harmonizes with ISO 14698 parts one and two.