For patient communities & health research
Gather your members’ experience with consent that means something, and access that you decide.
Few tools can show what someone agreed to, or check a later use against it.
Health data needs an application, a reasoned decision and a record.
With a rare condition, a small table can point to a family.
Each person chooses how their answers may be used, and can change it later.
A sale or a request includes only people whose terms allow it. Nothing leaves until you switch on sharing.
Your committee approves or declines each application with a reason, and every step is recorded.
Results and datasets hide small groups that could point to someone.
Tell people who asked about matching trials, in words that say nothing about their health.
Surdatics Verify checks for one real person per account, with no ID document. Your own address and brand on plans that include it.
Verify any dataset on the blockchain yourself. No account needed.
Verify on the blockchain →Surdatics is software for health studies, not a certification, and makes no study compliant on its own. You still bring your ethics approval, a lawful basis for health data, agreements with the researchers you approve, and a decision about where the data is hosted.
Who you need to hear from, how many, and where.
