Maryann Graham

Maryann Graham has extensive experience in regulatory affairs, having served as a Regulatory Affairs Specialist at Breckenridge Pharmaceutical, Inc. since 2016, focusing on regulatory submissions, labeling review, and CMC. Prior to this role, Maryann worked as a Regulatory Affairs Associate at Biodel Inc. from 2008 to 2016, where responsibilities included regulatory submissions, CMC, clinical operations, and analytical and bioanalytical assay validation. Earlier in the career, Maryann gained valuable experience at Bayer Pharmaceuticals from 1993 to 2008 in roles encompassing regulatory affairs, quality assurance, and analytical development.