Cleanroom monitoring systems to assure and certify sterility in cleanrooms and other isolated areas that require users to monitor, record, alarm and validate data. Stand-alone and graphic display models. With cleanroom monitoring systems, effective sterility assurance in cleanrooms and other isolated areas requires users to monitor, alarm and validate data as the three critical tenets of a comprehensive environmental monitoring plan.
Chemicals are used in a variety of industries in a variety of ways. Hazardous chemicals and chemical testing and processes require specially controlled cleanroom environments. These cleanrooms must adhere to ISO 14644-1 cleanroom classifications, and generally must meet a minimum classification of ISO Class 8.
The specialty chemicals market covers activities in which the use of specially adapted additives can add value to our clients’ products. Our expertise is based on our own cross-fertilisation strategy: our Application Laboratories follow the technical specifications and use or adapt additives from our various different sectors, from paper and textiles to paints. This approach allows us to offer new, stand-out solutions to our partners and clients.
Hospital cleanrooms can serve a couple of different purposes. One of these is to protect patients with compromised immune systems. Another is to serve as pharmaceutical cleanrooms in hospital pharmacies. In either instance, high levels of environmental control are required to protect patients’ health.
Medical research laboratories require strict cleanroom conditions. For example, for research involving blood or stem cells, an ISO Class 5/Fed Std 209E Class 100 to ISO Class 7/Fed Std 209E Class 10,000 cleanroom environment is necessary, per ISO 14644 standards. Other medical laboratories are subject to ISO 15189, which also has regulations of control of the laboratory environment.
As the world changes and new technologies develop, the aerospace industry is growing and increasing in relevance. The aerospace engineering and manufacturing industry is known for its high standards for both products and work environments due to the critical nature of aerospace products. Per ASTM E2352, aerospace cleanrooms must meet, at a minimum, ISO Class 7/Federal Standard 209 Class 10,000 requirements.
Plastic injection molding is crucial across so many industries, from automotive and aerospace to general manufacturing and medical devices. Quality is critical, so quality control cleanrooms, process control cleanrooms, and research and development labs are essential for plastic injection molders. Whether the components your company molds are for automotive, aerospace, medical devices, or something else, Angstrom Technology can design a cleanroom to meet your required standard: ISO 9001, ISO/TS 16949, ASTM...
The correct functioning of HEPA filters is normally tested at the time of installation, as well as part of the routine maintenance programme. It is normally recommended that HEPA filters are checked at 14 month intervals or less, or immediately after filter changing. Where high efficiency filters are fitted, it is vital that the filter housing/sealing device does not allow particulate material to pass and thereby compromise the cleanroom environment that is being served. Testing is necessary since HEPA filters...
Whether you’re cutting, welding, coating, grinding, or sanding, every metal fabrication task produces dust and fumes that can threaten your employees’ safety, derail productivity, increase maintenance costs, and place you in directly in the EPA’s crosshairs. Oil mist and dust particles can settle into every crack and crevice of your machinery, electronics, and cooling fans, eventually causing equipment failure and downtime. Who has the time and resources to redesign an entire facility around a...
The only complete Contamination Monitoring Solutions Provider. Since 1972, Particle Measuring Systems has been the global expert in contamination monitoring, providing the pharmaceutical and other life science industries with the expertise to detect, analyze and manage cleanroom contamination so you can meet all regulatory requirements including ISO 14644-1:2015 and EU GMP Annex 1.
ISO 14644-1:2015 continues to pose challenges to cleanroom managers and manufacturers. Here we provide several sources of information to help everyone from those new to this ISO regulation to veterans in the field. Our team of regulatory experts have put together a package of information so you can easily understand the requirements and what you need to do to meet them. Get a summary of ISO 14644-1:2015 by reading the paper below or watching the recorded webinar at the right. We also have FAQs and a paper to...
Providing you with a complete spectrum of contamination monitoring solutions. The Cosmetics and Personal Care manufacturing industry is required to meet ISO 22716:2007 and worldwide GMP Standards for hygienic production and contamination control. This includes monitoring viable and non viable contamination that could impact the safety and quality of your products. Particle Measuring Systems brings in-depth knowledge of manufacturing processes and regulatory codes, such as ISO 22716, to Cosmetics and Personal Care...
The Cleanroom is a combined laboratory chemical, mechanical and / or electronic whose main characteristic is the presence of very pure air, that is a very low content of fine dust in suspension. In the process of semiconductor production, the airborne particles (micro-powder) go to irreparably damage the micro-photoetched that form the chip, creating an electronic circuit defective, and then discarded. This process has forced the improvement of industrial production environments, removing particles from the air,...
Humidity control is an important factor for stable and predictable pharmaceutical production. From R&D labs to bulk production, humidity can affect both the chemical and mechanical properties of formulations, which can lead to quality issues and Good Manufacturing Practice (GMP) challenges. Laboratory and pharmaceutical product dehumidification systems can be the right solution to help prevent moisture issues during the production process for tablets, capsules, powders, and strips.
based in Amesbury, MASSACHUSETTS (USA).
The ambient air in clean air rooms needs to be constantly monitored for the safety of workers and of the production according to the environment. A clean air room is a room where the concentration of particles is controlled in order to minimize the introduction, the generation, retention of particles inside, for instance for chip production or the production of medicines.
Focuses on medium NOx, NOx-related and multigas-concentrations up to 5’000 ppm where flexibility is a central requirement. Parameters included are NO, NO2, NOx, NH3, NOx-amines, O2 and CO2. Typical supported applications are industrial emission monitoring and gas manufacturing control.
Focuses on low NOx and NOx-related concentrations up to 100 ppm where high resolution is required. Parameters included are NO, NO2, NOx and NOy. Target applications are ambient air monitoring, indoor measurement, clean room measurement and atmospheric research.
We provide different sizes of desiccant wheel.
Besides standard dimenions (diameter and thickness), non-standard wheels can be customized according to custmers' requirements, such as 50mm, 65mm, 100mm and 150mm.