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Directly from the manufacturer
3 June 2026 | 11:30 AM AEST
Join Testo Australia's Pharma Business Unit Manager, Dirk Macky for a practical session on environmental monitoring in highly regulated biotech environments. Covering compliance requirements, common failure points, and real-world best practices.
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What you will learn
Designed for quality, compliance, and laboratory professionals working in regulated biotech environments across Australia.
Why monitoring matters in biotech
Understand the compliance and quality drivers behind environmental monitoring requirements in regulated biotech settings.
Key industry and regulatory challenges
Navigate the regulatory landscape, including GxP, GMP, and 21 CFR Part 11 requirements for environmental data integrity.
The impact of poor monitoring
Understand how monitoring failures affect product quality, batch integrity, and your compliance standing with regulators.
Critical measuring points
Identify where to monitor temperature, humidity, pressure, and other parameters across labs, sample rooms, and fridges.
Common risks and failure points
Learn which monitoring gaps are most frequently cited in audits and how to address them before they become compliance issues.
Best practices from real biotech applications
Practical guidance drawn from Testo's experience supporting biotech facilities, including how Testo solutions can support your strategy.
Who should attend
This session is designed for anyone responsible for environmental monitoring, quality systems, or compliance in a biotech or life sciences environment.
Quality Managers and QA/QC professionals
Regulatory and compliance officers
Laboratory scientists and technicians
R&D and biotech researchers
Procurement and operations managers responsible for monitoring systems
Anyone evaluating or upgrading their environmental monitoring setup
Ready To Register
Secure your place for 3 June 2026 at 11:30 AM AEST. On-demand replay available