Google
Trusted Resources: News & Events
Latest announcements and gatherings
RARE Drug Development Symposium
The RARE Drug Development Symposium is a two-day interactive event in partnership with The Penn Medicine Orphan Disease Center that focuses on educating both beginners and advanced participants on the drug development process. Here, all members of the rare disease community are encouraged to explore their role in the rare disease drug development process in new and innovative ways.
This personalized experience is dedicated to empowering the rare disease community to continue to push forward on necessary treatments and cures, despite experiencing setbacks as a result of COVID-19. We are excited to offer poster presentations and speakers on engaging new topics, including CureAccelerator Live!
Date:
June 9 – 11, 2021
Location:
Virtual Event
This event has ended.
+myBinderRelated Content
-
Sickle cell disease and educationIt is often observed that sickle cell di...
-
2020 RARE on the Road – Virtual EventSince 2017, Global Genes and the EveryLi...
-
Camp SunshineFounded in 1984, Camp Sunshine provides ...
-
Living With Unpredictable Pain: A Sickle Cell Disease StoryGrowing up, Vismel Marquez wanted to joi...
-
Sickle Cell Disease: Treatments – PAINWeekhttps://www.youtube.com/watch?v=llqCdRNK...
-
How My Parents Set Me Up for Success in Sickle Cell ManagementMy parents knew they were carriers of th...
-
Northeast Louisiana Sickle Cell Anemia FoundationThe Northeast Louisiana Sickle Cell Anem...
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.