To guarantee the safety and efficacy of products manufactured in cleanroom environments, organizations such as International Organization for Standardization (ISO) and regulatory bodies such as the ...

In crucial areas, the majority of the recent regulations promote the use of continuous viable air monitoring. The BioCapt ® Single-Use (BCSU) Cleanroom Microbial Monitor by Particle Measuring Systems ...

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Positioning itself as a one-stop industrial testing equipment solution provider, Zetron has carved a dominant niche in the particle counter market. With nearly two decades of dedicated focus on gas ...

In the pharmaceutical industry, cleanrooms are categorized based on the level of airborne particle concentration necessary to meet the cleanliness standards required for the specific manufacturing ...

Biopharmaceutical manufacturing relies on many advanced technologies. Still, many pharma companies have room to improve when it comes to taking full advantage of everything modern tech has to offer.

To meet the requirements of regulatory agencies, pharmaceutical products are produced in a controlled setting. One example of such a controlled environment is a cleanroom, which is used to minimize ...

At the forefront of medical innovations, medical device manufacturers have undergone a remarkable transformation in recent years, driven by technological advancements and heightened demands for ...

Testo has also added more flexible webhook controls, enabling users to activate or deactivate webhooks without deleting existing configurations, reducing the time needed to reinstate them. Additional ...

Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...