The Invitae Patient Insights Network (PIN) is more powerful than a traditional patient registry. It's an online platform where individuals can take surveys, upload medical records, track health outcomes, and learn about the latest research and clinical trials.
PIN data is safeguarded and de-identified, which makes it possible to share it with researchers and biopharmaceutical companies working to help find new and better treatments for disease. Data is also shared with patients, giving PIN participants the opportunity to learn how others are managing similar health challenges.
What happens when I join?
As an Invitae PIN participant, you can take health surveys, upload medical records, and maintain your privacy while learning about the latest research and clinical trials. You own your data. You opt in and decide what to share and when you want to be contacted. After you take a survey, you can see responses and learn how others manage similar health challenges. De-identified data is also shared with researchers and companies working to improve care and find cures for diseases like yours.