MEDICAL INTELLIGENCE FOR DEVICE AUDITS

Evidence drives
safer decisions.

Veritas connects documents, clinical findings, approved product uses and regulatory sources in a traceable analysis. More clarity for the medical auditor to decide.

Human decision preserved Traceable evidence
ANALYZE. COMPARE. SUBSTANTIATE. SIMPLIFY.REAL EVIDENCE × HUMAN DECISION
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VERITAS / MEDICAL INTELLIGENCE

Data. Science. Intelligence.
Real impact in healthcare.

Evidence drives a healthier tomorrow.

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01 / THE CHALLENGE

Complex cases need more than an automatic answer.

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 approach
01
TUSS/ROL · DUT

Regulatory coverage

Traceable rules organize procedure codes and mandatory coverage criteria under Brazilian regulation.

02
ANVISA · IFU

Product and approved use

Product registration alone does not establish that a requested clinical use is approved. Sources and uncertainty remain visible.

03
REQUEST · FINDINGS

Clinical context

The request and documented examination findings are compared with the available instructions for use.

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01 / CLINICAL CONTEXTMedical auditingClinical experience at the center
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02 / INFRASTRUCTURETraceable AI
Medicine and technology
working together
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02 / MEDICAL EXPERTISE

Technology with a clinical perspective.

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.

03 / THE WORKFLOW

Layered analysis.
A trail you can follow.

AI and automation accelerate evidence gathering; verifiable rules preserve consistency. The auditor remains responsible for the decision.

01

Receive the request

Documents are organized by case and extracted with traceable evidence.

02

Cross-check sources

Rules and governed sources support checks of TUSS/ROL, DUT, ANVISA, contracts and instructions for use.

03

Human review

The preliminary analysis supports the medical auditor; the professional remains responsible for the decision.

PROCESS VIEWFrom request to review
TRACEABLE
01
Documentsreceived and organized
02
Rules and sourcescriteria checked
03
Contextual analysisevidence compared
04
Human reviewauditor's decision

Conceptual workflow. Actual results depend on the documents and sources available for each case.

04 / TRUST

AI knows where to stop. The auditor takes over.

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.

05 / CONTRACT OPTIONS

Dedicated infrastructure.
Transparent reference prices.

Reference amounts include reserved GPU infrastructure per client. Machine profile, scope, volume and operational requirements are sized before contracting.

01DEDICATED ENVIRONMENT

Pilot

Validate a real workflow

Validate one priority workflow with a defined scope and close medical-technical guidance.

R$ 14,900per month, BRL
Initial setupR$ 19,900
Initial 90-day cycle
REFERENCE SCOPE
  • Dedicated project GPU environment
  • One scoped priority workflow
  • Assisted validation with your team
Discuss a pilot
03DEDICATED ENVIRONMENT

Network

For multiple units or teams

Plan a phased rollout with shared governance across units.

R$ 59,900per month, BRL
Initial setupR$ 79,900
Annual contract
REFERENCE SCOPE
  • Dedicated GPU capacity, sized to needs
  • Phased implementation plan
  • Scoped integrations and governance
Discuss scale
04DEDICATED ENVIRONMENT

Institutional

For complex requirements

Isolated architecture and specialized implementation for institutional needs.

From R$ 99,900per month, BRL
Initial setupFrom R$ 149,900
Annual proposal
REFERENCE SCOPE
  • Exclusive GPU environment
  • Agreed security and operations
  • Scoped integrations, SLA and governance
Request a proposal
Prices are indicative, in Brazilian reais. GPU capacity, storage, case volume, integrations, taxes, availability and SLA are specified in a proposal. Setup is a one-time charge.
06 / NEXT STEP

Let's understand your operation before proposing a solution.

Discuss your workflow, sources and audit criteria directly with the Veritas team on WhatsApp.

No automatic authorization.
Evidence and human oversight.
BUSINESS CONTACT

A direct conversation about your needs.

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.
07 / FREQUENT QUESTIONS

Clarity from the first conversation.

Does Veritas authorize medical requests?

No. It organizes evidence and checks to support analysis. The medical auditor remains responsible for the conclusion.

Does Veritas replace official regulatory sources?

No. Official sources and governed rules take priority. Alternative sources are identified as secondary, never silently substituted.

What do the reference prices include?

A dedicated GPU environment is included in the reference pricing. Capacity, cases, storage, support, integrations, taxes and SLA are defined in the proposal.

Can Veritas integrate with any environment?

Each institution's integration, security and deployment needs require evaluation before a proposal. The site does not claim universal plug-and-play integration.