Advanced Clinical Research and Clinical Trials

Biography

Mona Dawood is Head of the Pharmaceutical Operations & Regulatory Affairs for CIDP group. She completed BSc (Hons) in Biomedical Chemistry from University of Warwick (UK) and a Diploma in CRA from Sup-Santé, Paris, France. She joined CIDP seven years ago and has acquired a significant expertise in specific monitoring in various therapeutic areas (oncology, diabetes and pediatrics). She has also an excellent knowledge of the European & Asian regulations, regulatory aspects, claims validations, pharmacovigilance

Abstract

Abstract : Conducting a clinical trial in Mauritius: Legal, regulatory and ethical frameworks