Methodology
How Quorenne structures educational procedure records—without diagnosing, determining candidacy, or teaching procedures.
Procedure Intelligence is for learning only. It does not decide whether a procedure is right for you—a qualified clinician should review your goals, history, skin, and medications.
Purpose
Procedure Intelligence helps users prepare for informed clinician conversations. It does not replace medical evaluation, prescribe treatment, rank clinicians, or predict outcomes.
Evidence hierarchy
- FDA and other relevant regulators
- Official device or product labeling
- Peer-reviewed systematic reviews
- Professional medical-society guidance
- High-quality clinical trials
- Clearly labeled expert consensus
Clinic marketing pages and promotional before-and-after claims are not treated as evidence.
Regulatory language
Quorenne preserves distinctions among approved, cleared, authorized, off-label, unapproved, not regulated as a medical device, varies by product/indication, and not yet verified. “FDA approved” is never used as a generic synonym for all devices or uses.
Editorial publication rules
Published records must include verified regulatory context, evidence provenance, meaningful risks, limitations, clinician questions, and an editorial status. Incomplete records remain in editorial review and do not appear in the public library.
Currently published: 25. Held for editorial review: 1.
Privacy
Phase 1 does not collect new medical-history, medication, pregnancy, diagnosis, or procedure-history fields. Procedure interests are not saved to Passport in Phase 1.