Pipetting and liquid handling sit at the heart of nearly every laboratory result, yet they are often overlooked when it comes to compliance and quality oversight. Small errors in volume delivery can compound across a workflow, affecting data quality, reproducibility and ultimately the decisions that depend on those results. In regulated environments, that risk carries real consequences during audits and inspections. This webinar explores the requirements laboratories need to understand to maintain compliant and defensible pipetting and liquid handling practices. The featured speakers will walk through the standards and guidance that shape expectations in pharmaceutical, biotech, clinical and research settings, and translate them into practical steps that can be applied right away. Topics include instrument qualification, calibration and performance verification, method validation, data integrity and building a quality program that holds up under scrutiny. The speakers will share real examples from the field, common pitfalls they see in the lab and straightforward strategies to close compliance gaps before they become findings. Whether managing lab operations, overseeing quality, developing methods or handling regulatory affairs, attendees will leave with clear guidance on how to strengthen confidence in results and maintain audit readiness. Register for this webinar to learn how pipetting controls can strengthen data integrity, regulatory compliance and inspection readiness.