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Can your cleanroom contamination control strategy protect product quality, meet EU GMP Annex 1, and reduce environmental impact? Join our webinar with experts from the Alliance for Sustainable Cleanrooms (ASC) to see how.

What most people miss about cleanroom differential pressure monitoring. Learn how differential pressure monitoring affects measurement certainty, alarming, and audit defensibility in regulated cleanroom environments. In this webinar we describe why the method of monitoring differential pressure...

In this webinar, you'll learn how to reduce update risk and downtime with a clear, documented approach to planning, executing, and verifying a viewLinc update. Vaisala's Senior GxP Regulatory expert provides a practical update workflow for viewLinc users, with validation considerations, risk...

Join Vaisala's Tamara Murusidze and guest speaker Yik Lam of Biogen to learn how inline refractive index supports confident protein concentration monitoring in ultrafiltration/diafiltration (UF/DF) and single-pass tangential flow filtration (SPTFF) processes. You will learn where conventional...

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.