Patient Advocacy Summit 2020

November 12, 2020 10:30 AM - 3:00 PM

Online Conference, Link will be sent in advance of the event.

Add to Calendar 11/12/2020 10:30:00 AM 11/12/2020 3:00:00 PM Patient Advocacy Summit 2020

MassBio's Patient Advocacy Summit brings together the patient advocacy community to showcase best practices and cutting-edge examples of how life sciences companies can more fully incorporate the patient voice into the work they do—not just approaching regulatory applications or at commercialization, but throughout the drug development cycle.

The program includes panel discussions, case study presentations(spotlighting industry/patient partnerships), and an inspirational keynote address.

See sponsorship opportunities here.

NOTE: MassBio makes every effort to accommodate our entire community at each of our events. Please let us know at least 3 days in advance of the event if you require special accommodations, such as captioning.

Online Conference, Link will be sent in advance of the event.
Executive Director and Global Rare Disease Patient Advocacy Lead, Pfizer
Katherine Beaverson, MS, is a Executive Director and Global Rare Disease Patient Advocacy Lead for the Rare Disease Research Unit (RDRU), at Pfizer Inc., leading the strategic planning and implementation of collaborations with patient advocacy groups in support of mutual areas of priority. She is external facing, engaging with rare disease patient advocacy groups to integrate their expertise into early medicines research and development. She is also internal facing, helping to facilitate alignment among cross-functional colleagues committed to advancing Pfizer science and programs with rare disease patient communities. Prior to joining Pfizer Inc., she held similar positions at Boehringer Ingelheim and Amicus Therapeutics. She is professionally trained as a Genetic Counselor, having spent 10 years at both New York Hospital- Weill Cornell Medical Center and Memorial Sloan-Kettering Cancer Center before entering industry. She received her BA from Swarthmore College and her Master of Science in Human Genetics from Sarah Lawrence College. Katherine is the current Chair of the Companies Constituent Committee of the International Rare Disease Research Consortium (IRDiRC) and a Member of the New York University Pediatric Gene Therapy Medical Ethics Working Group (PGTME).

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