Upgrading equipment or modifying workflows in the quality control (QC) lab can feel overwhelming, especially for microbiologists who may be unsure of where to begin or how to ensure compliance from the start. Without proper planning, even well-intentioned improvements can lead to unexpected regulatory gaps and costly rework.
This webinar offers a practical approach to navigating lab upgrades with confidence. Gain insight on pre-implementation considerations from a former FDA unit supervisor and analyze a case study of a laboratory that changed its final sterility release test. Designed as a “prep-before-you-step” guide, industry experts will share critical knowledge that will empower you to make informed, compliant, and efficient lab improvements.
Key takeaways include:
- How to approach regulatory agencies for planned changes in your QC micro lab
- Actionable insights for Celsis® rapid method adoption in your own lab via analysis of a Baxter Round Lake case study
- Regulatory expectations for implementing rapid microbiological methods in alignment with USP <73>
