Danna M. is currently the Director of CMC Regulatory Affairs at Chimerix, Inc., overseeing multiple pharmaceutical projects. Previously, they held the role of CMC Regulatory Project Manager at GlaxoSmithKline, responsible for post-approval regulatory strategies and project management for mature products. Danna has extensive experience in analytical R&D, having led teams in method development and validation for semi-solid products at Tergus Pharma. With over 17 years in the industry, they have demonstrated expertise in product development activities and regulatory submissions, contributing to critical initiatives for major pharmaceutical companies. Danna earned a Bachelor of Science in Chemistry from Lamar University.
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