Produce reviewable evidence for clinical AI workflows.
Your health system runs AI documentation, decision-support, and triage tools. Planisphere records the review around those clinical AI workflows: gate the boundary action, route a named human, seal the record — mapped to FDA PCCP and §1557 review while charts and PHI stay inside your network.
The record crosses the boundary. The chart never does.
When a regulator, a payer, or your own quality committee asks how the health system supervised its clinical AI, a written policy is a promise — a sealed record is evidence. Planisphere seals one tamper-evident record per gated action: hashes, decisions, timestamps, and the named human who signed off. The record carries none of the underlying chart, so the proof never touches PHI.
The medicine Toolkit: five primitives, pre-arranged.
The medicine Toolkit is the same five primitives — gate / route / seal / verify / meter — pre-arranged for PHI export boundaries and model-change evidence duties under HIPAA and FDA SaMD / PCCP. It is a catalog-backed pack bundle on the hosted API: record verbs plus the regulation catalog. See how the five primitives compose, or read the pack entry in the live registry.
Need the full medicine evidence map?
Use this page to decide whether Planisphere fits the workflow. Use the hub when internal or external compliance needs the complete inventory: 69 compliance anchors, 50 state routes, and comparison pages for health-system AI governance.