In the highly regulated pharma industry, ensuring that systems are validated and that information technology complies with legal and regulatory standards such as GxP, Sarbanes-Oxley, and CFR 21 Part 11 can be a challenge, even for the most experienced companies.
IMS's vast experience in the Pharma R&D space enables us to deliver systems that comply with the most stringent validation requirements and regulations. In addition, we support existing systems and their migration to compliant environments in preparation for external or internal audits.
