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About grappanetwork.org
To acknowledge the importance of patients in the development of recommendations for the management and/or diagnosis of psoriatic disease, GRAPPA created a Patient Research Partners (PRP) Network in 2012. In 2014 PRPs began to formalize a more coherent partnership cumulating with formal organizing documents and handbook in 2017. GRAPPA’s PRPs are comprised of patients from around the world who represent the patient perspective on GRAPPA working groups, committees, and research initiatives. The goal is to improve methodology and research outcomes and further the credibility of the results by affirming the treatment directive through the incorporation of the patient perspective.
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