Case Study: Leading Preclinical CRO achieves 3× better data quality and audit-ready compliance with Scispot

How a Preclinical CRO Achieved 3× Better Data Quality

Leading Preclinical CRO, a U.S.-based preclinical research and drug discovery CRO, faced fragmented spreadsheets and paper logs, GLP and 21 CFR Part 11 compliance risks, and time-consuming manual reporting and invoicing. To solve these digital lab management and regulatory challenges they adopted Scispot (Scispot Professional) to bring structure and consistency to their data and compliance processes.

Scispot implemented a centralized LIMS & ELN with automated compliance features (digital audit trails, electronic signatures), real-time instrument integration, and automated workflows. As a result Scispot delivered measurable impact: 3× improvement in data quality, a 50% reduction in labor hours, and 100% audit-ready compliance, while unifying teams, speeding study execution, and providing a scalable, future-ready platform.