Chirag has over 10 years Regulatory Affairs experience both within Clinical Research Organisations (CROs) and Pharmaceutical industry. He has in-depth experience of managing submissions for multi-country studies across Phases I, II & III and provides expert knowledge of local national requirements for the EU and Latin America.
Chirag has managed the preparation of a Marketing Authorisation Application (MAA) via decentralised procedure and filed US IND Applications.
In his academic career Chirag, a medicinal chemist, has conducted research into the synthesis and biochemical evaluation of inhibitors of estrone sulfatase as potential anti-tumour agents and completed his PhD at Kingston University.
