Join this exclusive webinar on the critical role of cleanroom design, regulatory compliance, and advanced monitoring systems in the life sciences sector.
In this session, Blake Hodess, CEO of Hodess Cleanrooms, will share insights from over 20 years of experience designing and building state-of-the-art cleanrooms that have driven breakthroughs in pharma, biotech, and high-tech manufacturing.
Paul Daniel, Senior GxP Regulations Expert at Vaisala, will discuss the pivotal role of viewLinc Continuous Monitoring System in ensuring GxP compliance and data integrity within life science environments.
What you will learn:
• Integrating compliance and Quality by Design (QbD) into cleanroom design
• Leveraging real-time monitoring to ensure GMP success
• Addressing the challenges of scaling cleanroom operations effectively
• Aligning facility design with FDA, ISO, and other regulatory standards across the product lifecycle
Who Should Attend:
• Director of Quality Assurance (QA)
• GxP Compliance Manager
• Facilities Manager
• Cleanroom Design Engineer
• Regulatory Affairs Specialist
• Validation Manager
