Become a Partner

Join us in the fight against psoriatic disease. Together we are stronger. Together we can improve the lives of all people affected by psoriatic disease!

IFPA is the global voice dedicated to advancing psoriatic disease policy. IFPA unites psoriatic disease stakeholders across sectors and geographies, partnering to strengthen national and regional capacity and leadership. IFPA works with others to generate and share evidence, informing change that can address the unmet needs of people living with psoriatic disease.

Together we have the power to transform and improve the lives of all people affected by psoriatic disease.

Unite. Strengthen. Lead.

Join us in our vision, A future where all people living with psoriatic disease enjoy good health and wellbeing, free from stigma and preventable disability and comorbidities.

Book a meeting for more information on how to become a partner: info@ifpa-pso.com

Our commitment:

  • Ensure global representation
  • Lead global advocacy
  • Strengthen Member capacity
  • Share knowledge
  • Unite stakeholders


The time for action is now

IFPA is the only global organization representing and uniting all people living with psoriatic disease – regardless of where they live, what type of psoriatic disease they have or how it impacts their lives. Despite many achievements over the past 50 years, people living with psoriatic disease continue to experience significant unmet needs. IFPA has worked hard to gain political support and recognition for people living with psoriatic disease and has received it. Now, it is time to move toward action and implementation. IFPA will keep advocating for psoriatic disease to receive greater recognition and push for countries to take responsibility for delivering on the recommendations set out in the Global Report on Psoriasis.

As partner you benefit from IFPA’s knowledge and draw on our 50 years’ experience of speaking up for people living with psoriatic disease.

IFPA's greatest strengths

  • Legitimacy to represent all people living with psoriatic disease: IFPA is the only organization that brings a unified global voice for all people living with psoriatic disease to the global agenda.
  • History and track record in the psoriatic disease community: For half a century, IFPA has been bringing together the psoriatic disease community and has a proven track record of elevating psoriatic disease on the global agenda.
  • Independence and integrity: Decisions are exclusively driven by the needs of people living with psoriatic disease.

Every new member makes the community stronger. Individuals, patient organizations, companies, trusts, and foundations all have a role to play.

Join us now!

Our partners

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  • So excited about the work being done around IFPA’s vision for the future and identifying the next “North Star.” IFPA continues to keep thing moving despite the pandemic and all the challenges arising from it.

    Cathy Ferrone

    Amgen

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We support ethical, accountable, and transparent collaboration with all our partners. Please read IFPA Code of Practice on Relationships with the Pharmaceutical Industry to learn more.