Nneka Onwudiwe PharmD PhD MBA | PRO/PE Regulatory Reviewer
US Government

Nneka Onwudiwe PharmD PhD MBA, PRO/PE Regulatory Reviewer, US Government

Nneka C. Onwudiwe, PhD, PharmD, MBA received her doctorate in Pharmacy (PharmD) from the University of Maryland School of Pharmacy, PhD in Health Services Research with a specialization in Pharmacoeconomics from the University of Maryland School of Pharmacy, and a MBA (Honors) from the University of Baltimore. In addition, she received an honor of Rho Chi in Pharmacy in 2002 and an honor of Beta Gamma Sigma in Business Administration in 2012. Dr. Onwudiwe is the technical expert and point of contact in the review of patient-reported outcomes (PRO), pharmacoeconomics (PE), and other type of claims in prescription drug promotion for the Division of Advertising and Promotion Review II (DAPR II) within the Office of Prescription Drug Promotion at the Food and Drug Administration (FDA). Dr. Onwudiwe teaches Comparative Effectiveness Research (CER) & Pharmacoeconomics at the University of Maryland School of Pharmacy. Dr. Onwudiwe has received several awards and accolades over the years. She has received funding as a Principal Investigator from NIH/NHLBI. Dr. Onwudiwe currently serves on the Food and Drug Law Institute (FDLI) Update Editorial Advisory Board and as a Workshop Review Committee Co-Chair for the International Society for Pharmacoeconomics and Outcomes Research (ISPOR), as well as a member of the ISPOR Value Assessment Frameworks Stakeholder Advisory Panel. Dr. Onwudiwe has served on several ISPOR Scientific and Health Policy Working Groups (Task Forces and Special Interest Groups) that have developed products and tools used by decision makers and researchers around the world. She is currently serving on the Value Assessment of Medical Device Special Interest Group. In addition to this work, Dr. Onwudiwe has presented at various professional conferences and published in several peer-reviewed journals such as Value in Health Regional Issues, Spine, Journal of the American Medical Association (JAMA), Obesity, Oncologist, Cancer Medicine, and Ethnicity and Disease. Dr. Onwudiwe holds a license in pharmacy and practices as pharmacist in the community providing medication therapy management (MTM) and other services.

Appearances:



Pharma Pricing & Market Access USA Day 1 @ 12:10

Communicating Medical Product Value at the Time of Market Authorization and along the Product Lifecycle

  • Develop a Target Product Profile (TPP) as a strategic development tool to identify desired  target concepts and facilitate communication regarding a particular clinical development program
  • Manage benefit-risk profile up to and beyond product approval by designing studies comprise not only of confirmatory clinical trials of efficacy or safety
  • Learn how to communicate the benefit-risk profile to external stakeholders that is consistent with the FDA-required labeling in a truthful and non-misleading way

Pharma Pricing & Market Access USA Day 2 @ 11:00

PANEL: Value based frameworks for precision medicine

  • Are current value frameworks suited to precision medicine?
  • What factors should be considered?
  • What are the ethical perspectives? 

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