We do projects on our own and in partnership and welcome you to present project ideas for further collaboration.
With our strong track record in patient education, advocacy, and awareness-raising, IFPA understands the complexity of psoriatic disease and shares its knowledge in patients' perspectives. Furthermore, IFPA offers access to our expertise and our global network of patients and patient associations.
All projects are conducted according to IFPA’s code of conduct and ethical rules.
About IFPA projects:
• Every IFPA initiative is assigned a Project Leader, fully responsible for planning, carrying out and reporting on project goals and outcomes
• Participating partners receive regular updates and full insight on the project
• Project funding is fully restricted. All funding is strictly used for the specific project
• IFPA projects are displayed on the IFPA website with their contributing partners