Quality Assurance

Quality is at the core of everything we do at ABS Clinical Solutions. Our independent Quality Assurance (QA) services are designed to ensure that your clinical trials, data, and processes adhere to the highest standards of regulatory compliance and scientific integrity. Our QA team conducts comprehensive audits across all phases of clinical development, including investigator site audits, vendor audits, internal system audits, and clinical study report (CSR) audits. We verify adherence to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and relevant regulatory requirements. We also provide expert consultation on quality management systems (QMS) development and implementation, SOP writing and review, and audit readiness support for regulatory inspections. Our objective is to identify potential compliance gaps, recommend corrective and preventive actions (CAPAs), and help you maintain a state of continuous inspection readiness, thereby minimizing risks and ensuring the credibility of your research.