Mona has a Bsc (Hons) in Biomedical Chemistry from the University of Warwick (UK) and a Diploma in CRA from Sup-Santé, Paris, France. Ever since Mona has returned to her home country Mauritius, she strives to bring forward the expertise and knowledge in the field of Science. With more than 5 years of experience in the field of research, monitoring and Trial Management, she gained her Clinical Research Associate Diploma in France in 2012 and monitored Oncology trials.
After working for 2 years in Regulatory Affairs, it was identified that there is a niche to develop a department dedicated to this field at CIDP. Due to her multidisciplinary qualities, Mona developed the department of Regulatory Affairs at CIDP. She has a good background in European Regulations, Mauritian Regulatory Aspects, Claims validations, cosmetovigilance and pharmacovigilance.
Mona works in close collaboration with toxicologists to overcome the risks and advice you on regulatory aspects of your projects. She is part of the CIDP scientific committee and advises on the choice and design of your research and development projects.