Trust

Trust is tiered.

Every record in MedevIQ carries a tier — A1, A2, or A3 — that tells you exactly how it was verified and against what. The tier travels with the record across every API call, every export, every cited reference. It is the floor your team should set for the decisions a record will inform.

The three tiers
A1
Expert verified
Three or more authoritative regulators agree, and a domain expert has reviewed the record. The floor for procurement contracts, regulatory submissions, and clinical-device decisions.
A2
AI reviewed, cross-source matched
Two or more authoritative regulators agree on the record's identity and classification. AI-reviewed for internal consistency. Production-grade for regulatory-affairs and procurement workflows.
A3
AI reviewed, single-source
One authoritative regulator. AI-reviewed for internal consistency, pending cross-regulator verification. Reference-grade — cite as such, never as a final regulatory claim.
Distribution today
A2
A3
A1 expert verifiedA2 cross-source matchedA3 single source

MedevIQ launched as an AI-reviewed canonical layer over nine regulators. Records start at A3 and move up to A2 as cross-regulator joins land, and to A1 as regulatory-affairs review catches up. Bar above is directional; per-tier record counts published at v1 launch.

Worked examples
A1ILLUSTRATIVE
Medtronic insulin pump (Class C / 510(k) K-cleared)
CDSCO + FDA + EUDAMED + Health Canada + TGA agree on classification, manufacturer identity and risk class. Expert review of MAUDE signal severity and recall history complete.
A2ILLUSTRATIVE
Mid-market ECG monitor (Class B)
FDA 510(k) + CDSCO manufacturing licence cross-matched. EUDAMED registration verified. Manufacturer-canonical resolved across spelling variants. Expert sign-off pending.
A3ILLUSTRATIVE
Recent CDSCO-only import licence
Indian importer registered with CDSCO; no global cross-reference yet (manufacturer outside the FDA/EUDAMED scope so far indexed). AI-reviewed for internal consistency.
Source authority hierarchy
REGULATORS
CDSCO · US FDA · EUDAMED · Health Canada MDL · TGA ARTG · PMDA · MHRA · NMPA · ANVISA
STANDARDS
GMDN · UMDNS · HSN · BIS Indian standards
SAFETY
FDA MAUDE · EUDAMED FSCA · Health Canada incidents · FDA recalls
Security & compliance posture
DPDP Act 2023(India)
Applicable · data processing within compliance scope
GDPR(EU customers)
Applicable · DPA available on request
HIPAA(US healthcare)
Not applicable · no PHI processed (reference data only)
SOC 2 Type I
On roadmap · Q4 2026 target
SOC 2 Type II
On roadmap
ISO 27001
On roadmap
Audit log access
Every record change and access event logged.
Available at the Enterprise tier — queryable via API or exported to your SIEM.
Pricing
Incident history
Live uptime and incident log.
Public status page with current incidents, resolution timeline, and rolling 90-day history.
Status
Early access

MedevIQ is in private preview.

We're onboarding hospitals, manufacturers, regulators and research teams in waves. Tell us how you'd use MedevIQ and we'll get back within a working week.

We'll reply within a working week.

Access by invitation while v1 finalizes.