management systems, and electronic training management systems. Its products support clinical trial planning and execution, document and signature management, remote source data verification, investigational medicinal product tracking, and electronic signatures. TechyPharma focuses on regulatory requirements such as FDA 21 CFR Part 11, ICH-GCP, HIPAA, GDPR, and related standards. Its solutions are used to manage data integrity, automate quality workflows, and support audit and inspection readiness across life sciences operations. The platforms are designed for multi-site trials and enterprise-scale research environments.