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Join our free webinar to learn best practices for placing temperature, humidity, CO₂, and differential pressure sensors in regulated environments—so you’re always ready for audits and inspections.

In this 45 minute training session, three industry experts explain why validation is not just a regulatory checkbox for 3PLs, but a practical tool to demonstrate operational control to pharma, medical device, and biotech clients.

This webinar covers essential strategies for GxP cleanroom success, including compliant facility design, Quality by Design principles, and real-time monitoring for GMP. Industry experts Blake Hodess and Paul Daniel share guidance on scaling operations, meeting FDA/ISO standards, and setting up your...

In this session, Vaisala’s Paul Daniel, GxP regulatory expert, explores how adaptable environmental monitoring systems help small-scale, high-speed cell and gene therapy (CGT) and Advanced Therapy Medicinal Products (ATMP) facilities maintain compliance as they grow.

In hospitals and clinical settings, environmental parameters like temperature, humidity, pressure, and CO₂ directly affect patient safety, clinical workflows, and regulatory compliance. In this webinar, Vaisala’s Senior GxP Regulatory Expert shows what a fit-for-purpose continuous monitoring system...

Join Vaisala experts Joni Partanen and Anniina Uotila for an in-depth look at CO 2 measurement and control in CO 2 incubators. We’ll explore the role of incubators in applications such as cell culture and tissue engineering, and why CO 2 stability is critical for cell viability and reproducibility.

Join us for a webinar on advanced clean room monitoring in cell and gene therapy. Learn about EMS independence, risk-based sensor placement, validated solutions, wireless data loggers, compliance, and best practices for reliable, efficient, and compliant environmental monitoring.

Cleanrooms are mission-critical environments where control, compliance, and cleanliness are everything. But as industries face growing pressure to meet both regulatory and environmental demands, how can cleanrooms be designed for long-term sustainability without compromising performance?

Learn how to optimize vaporized hydrogen peroxide bio-decontamination processes for aseptic isolators. In this recorded webinar, we'll show how to maximize efficiency and minimize downtime by using the Relative Saturation value . This session is designed for professionals in the pharmaceutical and...

While standard solutions work for most environmental monitoring needs, some applications require a more customized approach. If your facility has unique measurement challenges or specialized configurations, an Engineered-to-Order (ETO) monitoring solution may be the right fit.