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.
Speaker
Nicholas Enea, Product Manager, Artel MVS, Nova Biomedical
Nick Enea is the Product Manager for the Artel MVS under Nova BioMedical. With more than 10 years of experience as a Laboratory Applications Scientist with Artel, Nick brings deep expertise in genomics, immunoassay development and regulatory compliance. Having worked in the molecular diagnostics and instrumentation space, Nick understands the issues involved with taking a regulated product from research to the market and uses this experience to help find meaningful solutions for customers’ liquid handling challenges. He is qualified to comply with the requirements of ISO/IEC 17025.
Message PresenterWho Should Attend?
This webinar will appeal to:
- Lab Managers
- Quality and QA professionals
- Scientists
- Method Development and Automation teams
- Validation Engineers
- Regulatory Affairs staff working with manual or automated liquid handling
What You Will Learn
Attendees will gain insight into:
- The regulatory landscape and standards that apply to pipetting and liquid handling
- Practical approaches to calibration, verification and ongoing performance monitoring
- How to support data integrity and produce defensible results
- Where compliance gaps typically hide and how to address them
- Ways a quality-driven liquid handling program improves reliability and inspection readiness
Xtalks Partner
Nova Biomedical
Advanced Instruments and Nova Biomedical are now doing business under the same brand, bringing together decades of expertise in analytical instrumentation, R&D, and global customer support. The Solentim® ecosystem is now part of Nova Biomedical’s portfolio, providing best-in-class imaging and single-cell deposition technologies for cell line development workflows and assurance of clonality for regulatory bodies.
You Must Login To Register for this Free Webinar
Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.
Create Account