This webinar will guide you into the journey of data, with a specific focus on Environmental Monitoring Systems for pharmaceutical cleanroom.
What You’ll Learn:
Dig into the design, implementation and validation of an Environmental Monitoring System with essential steps to ensure the generation of meaningful data. We’ll describe best practices that enable data to become “information”, and support improvement or corrective decisions.
- How to ensure your Environmental Monitoring System is properly designed and validated, with specific reference to the selection of sampling point and risk based approach
- How to properly configure alert and action limits, and ensure a continuous adjustment/improvements of them, according ISO standards
- How to make multidimensional analysis of data, to identify contamination root cause and generate CAPA
Who should listen to this on-demand webinar
All Pharmaceutical cleanroom users, especially those working in the following departments:
- Quality Assurance
- Quality Control
- Information Technology