Clintask delivers full-spectrum Computer System Validation (CSV) solutions across laboratory, manufacturing, and clinical systems, ensuring compliance with FDA, MHRA, and ICH GxP standards. Our risk-based validation methodology aligns with CSA principles, supported by Data Integrity (ALCOA+), 21 CFR Part 11, and Annex 11 frameworks. We also integrate GMP, GLP, and GCP audit readiness, enabling sponsors and CROs to achieve continuous regulatory assurance.