Improve Regulatory Compliance for Pipetting and Liquid Handling Workflows

Date
Tuesday, September 01, 2026Tue, Sep 1, 2026
Duration
60 min
Ready On-Demand
Free — start watching in secondsFree

About this webinar

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.

Who should attend

  • 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

  • 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

Featured Speakers

Nicholas Enea, Product Manager, Artel MVS®, Nova Biomedical

Nicholas Enea

Product Manager, Artel MVS® · Nova Biomedical

Nick Enea is the Product Manager for Artel MVS® at 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 challenges of taking a regulated product from research to market and uses this experience to help customers find meaningful solutions to their liquid handling challenges. He is qualified to comply with ISO/IEC 17025 requirements.

Partner for this event

Nova Biomedical

Advanced Instruments and Nova Biomedical now operate under the same brand, combining decades of expertise in analytical instrumentation, R&D, and global customer support. Nova Biomedical provides scientific and analytical solutions for bioprocessing, spanning cell culture monitoring, cell line development, liquid handling quality assurance, osmolality testing, and process optimization to help biopharmaceutical organizations increase efficiency and advance scientific discovery with confidence.

On-demand webinar