
Tel: 301.424.9700 · Fax: 301.296.4751 · Email: info@grs-cro.com · Other locations

GRS’ Quality Assurance (QA) Department has well-established and defined procedures for its Document Control System, Standard Operating Procedures System, Corrective and Preventive Action System, and Review and Audit System. QA monitors the activities for the Trial Master File (Regulatory Binder) and reviews and approves the clinical study reports prior to submission to our clients.
QA has a strong history of working with regulated departments throughout GRS to successfully address any compliance issues that may arise whether global or regional in nature.