Ritika Dhanda

Ritika Dhanda is a Senior Regulatory Affairs Program Lead at Johnson and Johnson, bringing over ten years of experience in the medical device industry. They hold a Master's in Biomedical Regulatory Affairs from the University of Washington and have previously worked as a Senior Regulatory Affairs Specialist at BD and a Regulatory Affairs Specialist at Philips. Ritika has a diverse background, having served in various regulatory roles, including as an Independent Regulatory Consultant and a Regulatory Affairs Executive. With extensive knowledge of regulatory strategies and compliance, they are skilled in both U.S. and international regulatory requirements.