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Semiconductor makers rely on airborne particle counters to keep cleanrooms pristine. Even the tiniest particle can throw off chip quality and production yield. That’s why every detail counts when building the world’s most advanced technology.
Environmental monitoring in aseptic pharmaceutical manufacturing involves regular testing of the air and surfaces in the cleanroom to detect the presence of any contaminants that could pose a risk to the production process.
Continuous air monitoring in Grade A cleanrooms means checking for live germs in the air the entire time critical work is happening-like setting up equipment or handling products-to catch any contamination risk right away and keep everything safe for patients
Real Time Monitoring Systems (RTMS) in Cleanrooms are a necessity for the monitoring and contamination control in many applications. From Semiconductor to Pharmaceutical products RTMS provide real time data records and notifications of any environmental out of tolerance conditions.
In cleanrooms classified ISO 5 or cleaner, compressed gasses pose a serious risk of particle contamination. Thus, monitoring compressed gasses for contamination is a critical portion of the contamination control plan.
Due to an unforseen technical difficulty, we’ll be rerunning this webinar event on June 20, 2025
Learn about the latest EU GMP Annex 1 requirements for continuous microbial monitoring in aseptic processing area. Join us for a practical overview on how to set up environmental monitoring (EM) that keeps your process environment safe from microbial contamination — now easier than ever with Lighthouse’s ActiveCount Remote Impactor Kit.
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