Chirag Patel

Senior Director, Regulatory Affairs & Technical Writing

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 ย synthesis and biochemical evaluation of inhibitors of estrone sulfatase as potential anti-tumour agents and completed his PhD at Kingston University.

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