Navigating patient-reported outcomes (PROs) such as symptoms, treatment satisfaction, quality of life, and treatment adherence is a critical component of a patient-centric healthcare system. Increasingly, PROs are becoming a crucial element in the decision process for payers, providers — and even for securing FDA approval. But how can PROs actually advance healthcare and how can your organization put them to use?

Join experts from Cardinal Health in the first of a three-part webinar series on PROs, as they provide insight on the foundational elements of PROs and recent regulatory trends. Key objectives for our first webinar include:

  • The basics of patient-reported outcomes
  • FDA’s perspective on PROs, including current and future initiatives to expand usage
  • Key therapeutic areas leveraging PROs
  • PRO instrument development process

Featured Speakers

Todd Phillips, PharmD, RAC

Director, Global Regulatory Affairs
Cardinal Health Regulatory Sciences

Todd Phillips, PharmD, RAC, is Director of Global Regulatory Affairs for Cardinal Health Regulatory Sciences. Dr. Phillips provides strategic development and regulatory consulting services to a variety of drug and biological product manufacturers. He has more than 15 years of experience in regulatory affairs, drug development, clinical project management and product marketing. Prior to joining Cardinal Health in 2011, he gained experience at FDA and in varying positions in the pharmaceutical and CRO industries.

Marjorie Zettler, PhD, MPH

Senior Scientist
Cardinal Health Regulatory Sciences

Marjorie Zettler is a Senior Scientist for Cardinal Health Regulatory Sciences. She has more than 15 years’ experience in the pharmaceutical industry, focused on clinical research, product development and medical writing. Dr. Zettler received a doctorate in physiology and a bachelor’s degree (honors) in genetics from the University of Manitoba, Canada, as well as a master’s degree in public health from the University of Manchester, United Kingdom.

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