Nicola Kidman is a Principal Consultant, Regulatory Affairs at Arriello and has over 20 years of EU/UK and International regulatory experience gained via positions in pharma, CROs and consultancy companies. Her expertise spans all aspects of regulatory affairs from early drug development to post marketing support, including clinical trial applications and amendments, clinical development plans, scientific advice, Orphan Drug Applications, Paediatric Investigation Plans, MAAs, and life cycle maintenance support.
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