The Quality Assurance group at G7 Synergon is one of the key drivers, ensuring that the quality of services matches global standards. Our independent Quality Assurance unit provides audit services as part of

 study - specific quality strategies for the clinical trials, and internally as part of our company QA program. Our QA auditors emphasize on supporting project teams in their effort to conduct high quality clinical research work. Our QA program is embedded in the company’s Quality Management System (QMS).

Our QA Auditors Support the Following

• GCP/GLP Audits (In-process, retrospective & system audits)
• Investigator Site Audits
• Sponsor Audits
• Clinical and Analytical Laboratory Audits as per ISO 15189 & ISO17025
• SOP writing and reviewing
• ln house Files facility
• Adverse Event Reporting System Audits
• Computer Systems Validation Audits
• Database and Data Management Audits
• Final Report Audits
• Archival Audit

Quality Policy