Pharma Medica has internally developed an extensive proprietary suite of 21 CFR Part 11 compliant, validated software used for clinical trial management, data acquisition and analysis. Our Quality Assurance department’s Computer Systems Validation (CSV) team closely collaborates with users and our software development department to continuously enhance data assurance and reliability. Our commitment to digital advancements and automated data capture ensures that our clinical trials are conducted with precision and adherence to regulatory standards.

Pharma Medica assures data security through oversight of our network and implementation of security measures to prevent data loss, unauthorized access, and damage from a wide array of risk factors. Our data security is geared to protect the privacy and confidentiality of our sponsors, subjects, and staff. It also protects all intellectual property while maintaining the integrity and availability of our study data.

Quality Assurance oversight of operations is risk-based and provides proactive risk mitigation assurance. Process performance is our primary focus. Our Quality Management System and internal audit program ensure that process improvements aligning with global legislative standards are continually implemented.