Join us for an insightful webinar where you’ll explore the regulations driving pharmaceutical companies to perform environmental monitoring and see how this process can be transformed into a fully automated, paperless workflow across all instruments involved.
We’ll walk you through how a sampling plan and measurement process can be mapped once, seamlessly integrated into mobile units, and used to guide operators through daily measurements with precision. Thanks to a bidirectional interface, data entry errors are minimized, ensuring reliable results every time. Even active air monitoring can be done automatically, with robotic arms precisely positioning and operating air samplers to capture samples and transfer plates, eliminating manual intervention and human error.
All collected data is automatically uploaded into advanced environmental monitoring software, where routine results are instantly trended in pre-validated reports—already aligned with the requirements of major health authorities worldwide. Plus, this data feeds powerful AI tools designed for in-depth investigations and root cause analysis, helping you quickly identify and address issues.
By the end of this session, you’ll gain a clear, practical view of what’s possible today with validated systems that can be rapidly implemented in your facility—accelerating compliance, improving efficiency, and reducing human error.
- Understanding Automated Environmental Monitoring Workflows
- Regulatory Compliance and Data Management
- Application of Advanced Technology for Data Analysis
Webinar brought to you in partnership with
- QA Managers/Directors
- QC Microbiologists/Analysts
- Environmental Monitoring Specialists
- Compliance Officers
- Auditors
- Production Managers
- Process Engineers
- Automation Engineers
- Manufacturing Technicians working in sterile environments
- Validation Engineers
- Commissioning Engineers
