Information Age Systems

IAS provides a complete range of validation services for companies regulated by the FDA. These services include risk assessment, gap analysis, validation planning, and remediation. Whether it is the implementation of a new system or an audit and remediation of an existing application Information Age Systems can help. We utilize the principals outlined for Good Automated Manufacturing Practices, (GAMP) to help our customers adhere to computer systems validation requirements. IAS also has experience with Chapter 21 Part 11 Audit Trails and Electronic Records Signature requirements.