Regulatory coverage
Traceable rules organize procedure codes and mandatory coverage criteria under Brazilian regulation.
Veritas connects documents, clinical findings, approved product uses and regulatory sources in a traceable analysis. More clarity for the medical auditor to decide.

Evidence drives a healthier tomorrow.
A request can require document review, code verification, coverage rules and a comparison between clinical indication and approved product use.
Veritas organizes those steps into an explainable trail, showing both completed checks and questions that still need review.
See the approachTraceable rules organize procedure codes and mandatory coverage criteria under Brazilian regulation.
Product registration alone does not establish that a requested clinical use is approved. Sources and uncertainty remain visible.
The request and documented examination findings are compared with the available instructions for use.


Veritas does more than read documents: it relates the physician's request and examination findings to a product's approved use, while keeping sources and unresolved questions visible.
Medical-auditor CEO + computer-science PhD CTOMedical audit experience combined with engineering and computer-science research.
AI and automation accelerate evidence gathering; verifiable rules preserve consistency. The auditor remains responsible for the decision.
Documents are organized by case and extracted with traceable evidence.
Rules and governed sources support checks of TUSS/ROL, DUT, ANVISA, contracts and instructions for use.
The preliminary analysis supports the medical auditor; the professional remains responsible for the decision.
Conceptual workflow. Actual results depend on the documents and sources available for each case.
Veritas does not turn a probabilistic answer into an authorization. It separates evidence, rules and explanations, and makes gaps requiring review explicit.
TraceabilitySources, states and artifacts can be inspected.
Clear limitsA product registration is not proof of approved clinical use.
Human oversightSystem reports are preliminary; the professional decides.
Reference amounts include reserved GPU infrastructure per client. Machine profile, scope, volume and operational requirements are sized before contracting.
Validate one priority workflow with a defined scope and close medical-technical guidance.
Structure routine audits with a dedicated Veritas instance and reserved GPU infrastructure.
Plan a phased rollout with shared governance across units.
Isolated architecture and specialized implementation for institutional needs.
Discuss your workflow, sources and audit criteria directly with the Veritas team on WhatsApp.
If a plan interests you, its button above starts a conversation with that context.
+55 85 9126-5570Talk on WhatsApp WhatsApp opens in a new tab. This page does not collect your data.No. It organizes evidence and checks to support analysis. The medical auditor remains responsible for the conclusion.
No. Official sources and governed rules take priority. Alternative sources are identified as secondary, never silently substituted.
A dedicated GPU environment is included in the reference pricing. Capacity, cases, storage, support, integrations, taxes and SLA are defined in the proposal.
Each institution's integration, security and deployment needs require evaluation before a proposal. The site does not claim universal plug-and-play integration.