Andjica Tasic

Head of Quality Assurance

Andjica is a seasoned quality and compliance leader with more than 30 years of experience supporting regulated environments across the life sciences industry. She specializes in quality assurance, regulatory compliance and inspection readiness, with deep expertise in GCP, GLP/GCLP, GMP and ISO standards supporting Phase I–III clinical trials and bioanalytical studies.

Throughout her career, Andjica has led complex quality and compliance initiatives focused on operational excellence, risk management, vendor oversight and adherence to global regulatory requirements. She brings extensive experience supporting sponsors, CROs, laboratories and clinical sites through inspection readiness activities, quality system development, remediation efforts and regulatory inspections.

Andjica has successfully led and hosted numerous FDA and global regulatory inspections and is recognized for her proactive, solutions-oriented approach to quality management and compliance oversight. Her background includes extensive auditing expertise across clinical, laboratory, vendor and manufacturing environments.

She is a Certified Quality Auditor (CQA) through the American Society for Quality (ASQ) and a Certified Clinical Research Professional (CCRP), reflecting her long-standing commitment to quality, regulatory excellence and clinical research integrity.