Daphine Glowner is a Regulatory Associate for Pearl Pathways. Daphine has over a decade of experience in pharmaceutical and medical device regulatory document formatting and editing, project management, document publishing, eCTD, and quality assurance. She earned her B.A. in English from Indiana University-Purdue University Indianapolis.
Daphine’s current responsibilities for Pearl Pathways include serving as document manager for various projects, providing assistance with global Electronic Common Technical Document (eCTD) filings, providing QC services for regulatory filings, publishing support for IND/NDA/BLA/510k submissions, and editing documents to meet FDA standards. She is proficient in SharePoint, Adobe Acrobat Pro 11, and TRS Toolbox.