Google
Trusted Resources: News & Events
Latest announcements and gatherings
Rare Diseases and Orphan Products Breakthrough Summit
Each year, the NORD Summit, one of the largest multi-stakeholder events in rare disease, brings together participants spanning the rare community, including rare disease experts and leaders from patient advocacy groups, government, industry, and academia to discuss the most current and critical topics related to rare diseases and orphan products.
Date:
October 17-18, 2022
Location:
Washington, DC
This event has ended.
+myBinderRelated Content
-
Foundation for Women & Girls with Blood DisordersIn 2010, the Foundation for Women & ...
-
Carolinas Sickle Cell Collaborative (StepUp4Sickle)The Collaborative is a joint effort betw...
-
Data & Statistics on Sickle Cell DiseaseSickle cell disease (SCD) affects millio...
-
The State-of-the-Art Methodology Behind New Sickle Cell Disease GuidelinesSickle cell disease (SCD) is an inherite...
-
Global HOPE Initiative Plans $100M Pediatric Hematology-Oncology Treatment Network in AfricaThe Bristol-Myers Squibb Foundation, Tex...
-
Under The Radar: Sickle Cell DiseaseIn the U.S., an estimated 100,000 Americ...
-
ASH Clinical Practice Guidelines on Sickle Cell Disease (SCD)https://www.youtube.com/watch?v=tozUcTSN...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.