Renata. Zimova

Biography

Experienced Professionnel with over 14 years of QA and regulatory experience gained in EMEA, national regulatory authority and international company (GCP, GMP. Pharmacovigilance) - Extensive experience of management of health authority inspections including FDA, EMA & MHRA - Expert knowledge of clinical research and development of regulatory and GCP requirements - Excellent leadership, teamwork, communication and influencing skills across regions and cultures - Wide experience in GCP, GMP and Pharmacovigilance. Knowledge of ICH GCP, EU GMP

Research Interest

GCP, GMP and Pharmacovigilance. Knowledge of ICH GCP, EU GMP