Bioanalytical studies analyze biological samples to measure drug concentrations, biomarkers, and other critical data in clinical research. Precision, efficiency, and regulatory compliance are vital in bioanalytical studies, yet manual data recording and fragmented software often lead to errors and operational challenges. A laboratory information management system (LIMS) centralizes data, simplifies workflows, and ensures compliance, improving research reliability and productivity.
Download this case study to learn how a LIMS solution helped the Global Clinical Central Lab:
- Enhance data integrity and traceability by centralizing study data, eliminating paper records, and ensuring full audit trails for regulatory compliance
- Optimize quality assurance and reporting with automated study tracking, reducing the time for pharmacokinetics (PK) validation reporting
- Improve compliance and workflow efficiency by seamlessly integrating study-specific labeling and digital tracking, ensuring adherence to FDA and global standards
