DEBRA International is a worldwide network of national groups working on behalf of those affected by the genetic skin blistering condition Epidermolysis Bullosa (EB). Our vision is to ensure that people living with EB have access to the best quality support and medical care, while also driving the development of effective treatments and cures for EB.
One of DEBRA International's main activities is supporting research to gain a better understanding of the causes of all forms of Epidermolysis Bullosa (EB), with the aim of developing improved treatments and diagnostics and, ultimately, we hope, even cures.
Please check deadlines for submission carefully. When preparing your application please take into account that the administrative authority member of your host institution will be required to approve each completed application via the Grant Tracking online system prior to submission.