Prepare for impact.
We develop educational programs that prepare patients and care partners to apply their lived experience to inform the development of new and better medicines.
We develop educational programs that prepare patients and care partners to apply their lived experience to inform the development of new and better medicines.
We envision a future in which patients and their care partners are routinely engaged by drug companies, regulators and payers for their expertise throughout the development and assessment of every new medicine.
The Patients’ Academy for Research Advocacy is helping patients and care partners get ready to engage in research as full partners whose unique experience can advance science and medicine.
We educate patients and care partners in a first-of-its kind interactive training program that is open to all comers, regardless of the disease or condition they live with. Our programs are designed with and for patients, with input from drug developers, regulators and other stakeholders. Participants learn not only the basic process of developing drugs, but also how decisions are made by other stakeholders, and where and how the voices of patients can improve drug research and development by focusing it on products and outcomes that meet their needs.
Founder Susan Schaeffer spent 15 years educating industry about innovation in clinical development, regulation, pricing and market access.
We are an independent nonprofit whose success depends on partnering with like-minded patient groups and industry sponsors who share our vision for patient-centered R&D.