Home > Clinical Research > Quality assurance
Quality assurance PDF Print E-mail

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




India, an emerging global hub for vaccine industry ASIA is emerging as the vaccine hub ...


“G7 SYNERGON has been recognized by the Department of Scientific and Industrial Research (D...

Vaccine Industry in India – An Emerging Global Hub

Asia is emerging as the vaccine hub of the world and India is on the go to play a key role in the...

Post Marketing Clinical (PMC)

Phase IV Studies – A Market With A Proactive Approach For Growth Of A Pharmaceutical Busine...
Counter :mod_vvisit_countermod_vvisit_countermod_vvisit_countermod_vvisit_countermod_vvisit_countermod_vvisit_counter

© 2019 G7 SYNERGON. All rights Reserved