Mission
The Foundation for Cell & Gene Medicine is an independent, 501(c)(3) non-profit established in 2018, dedicated to providing the education, information, and research required to accelerate awareness and access to transformative therapies in cell and gene medicine.
Basic Information
Tax-Exempt
Founded in
Not Reported
EIN
30-0752401
Total Assets
$154.1 thousand
At a Glance
Foundation and RARE-X Release White Paper on Using Patient Owned Data
Explore the insights from our collaborative white paper focusing on patient-owned data to enhance gene medicine.
Webinar: Cell Therapies for COVID-19
Participation in webinars discussing innovative cell therapies in the fight against COVID-19.
Report: Healing Genes Nomenclature Summit
A report summarizing discussions from the Healing Genes Summit on nomenclature in gene medicine.
Past Events
RARE Health Equity Summit
Nov 17, 2021 – Nov 19, 2021
This event is for rare disease patient advocate organizations, non-profit stakeholders, industry professionals, and others who are looking to collaborate with other experts about health inequities.
Rare New England Annual Conference
Date not specified
ARM Foundation for Cell and Gene Medicine will have a virtual exhibitor booth at this event, where attendees will have access to our educational materials about cell and gene medicine.
Rare Diseases and Orphan Products Breakthrough Summit
Oct 17, 2021 – Oct 18, 2021
This event is for patient advocacy groups, government, industry, and academia to unlock new insights, network and discuss critical topics in the rare diseases and orphan products field.
Our Programs
Healing Genes
An educational initiative providing the public with accurate, jargon-free information about cell and gene medicine.
Learn MoreSTRiDE (State Rare Disease Education Initiative)
A program to engage and inform members of the rare disease community about cell and gene medicine.
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