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For laboratories subject to GLP, GMP and GCP requirements, managing pipette inventory, service scheduling and calibration records manually can be a challenge. Mislabeled pipettes, misread information and mistakes in manual data entry can be difficult to spot. These errors can significantly impact projects, especially in organizations managing hundreds or thousands of pipettes across multiple labs or sites.
Complying with FDA 21 CFR Part 11 regulation doesn't need to be an onerous task. Implementing an automated pipette management system aligned with critical regulatory requirements can play a key role in streamlining traceability and data integrity.
Download our white paper to learn more about how you can automate pipette compliance to stay audit-ready.
