Janet Maynard
Dr. Janet Maynard, as the Director of the Office of Orphan Products Development (OOPD), oversees legislatively mandated designation and grant programs intended to promote the development of products for rare diseases including, orphan drug, rare pediatric disease, and humanitarian use device designation programs, as well as clinical trial, natural history study, and pediatric device consortia grant programs. In her role, she serves as FDA’s lead in coordinating cross-cutting rare disease issues and engages extensively with patients, sponsors, and other stakeholders.
Americas
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Rear Admiral Richardae Araojo •
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Robyn Bent, MS, RN •
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Kevin Bugin •
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Namandjé Bumpus •
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Ashley Boam, MS •
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Diane Bruce, PharmD, RAC •
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Suranjan De •
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Michelle Campbell •
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Ethan Chen •
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John Concato •
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Jacqueline Corrigan-Curay, JD, MD •
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Christy Cottrell •
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Selena Daniels, PharmD, PhD, MS •
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Khair ElZarrad •
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Ron Fitzmartin, PhD, MBA •
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Dionna Green •
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Richard Forshee, PhD •
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Andrea Fristedt •
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Cheryl Grandinetti, PharmD •
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Karen Hicks •
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Sarah Ibrahim •
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Xianghong (Emily) Jing •
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Michael Kopcha, PhD, RPh •
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Jung Lee •
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Claudia Manzo •
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Peter Marks •
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Janet Maynard •
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Hilary Marston •
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Ann Meeker-O'Connell, MS •
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Monica Morell, PhD •
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Tina Morrison •
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Theresa Mullin, PhD •
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Monica Munoz •
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Iilun Murphy •
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Martha Nguyen •
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Steven Oh, PhD •
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Lee Pai-Scherf •
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Y. Veronica Pei •
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Ana Pineda Zavaleta, MSc •
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Andrew Potter •
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Dionne Price, PhD •
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Scott Proestel, MD •
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Francisca Reyes-Turcu •
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Stacey Ricci •
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Leyla Sahin •
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Norman Robert Schmuff, PhD •
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Kimberly Schultz, PhD •
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Haley Seymour, MS •
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Mary Ann Slack •
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Peter Stein •
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Mary Thanh Hai, MD •
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Julia Tierney •
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Melissa Torres •
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Stelios Tsinontides •
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Katherine Tyner •
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John Weiner, JD •
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Celia Witten •