Evidence Library: A Transparent Repository of Verification Data
Bottom line: the Evidence Library provides transparent, auditable access to all evidence sources used in our evaluations, with clear labeling of verification status and known limitations.
Purpose
The Evidence Library is the backbone of our evidence-centered evaluation approach. It provides:
- Source documents: Manufacturer brochures, technical specifications, IFU documents
- Verification status: Clearly labeled for each source
- Document analysis: Cross-referencing and discrepancy identification
- Audit trail: Track when evidence was reviewed and by whom
Evidence Source Types
1. Manufacturer Documents
- Technical specification sheets
- Instructions for Use (IFU)
- Product brochures
- Clinical study reports
- Regulatory certificates (NMPA, CE, etc.)
2. Independent Sources
- Peer-reviewed publications (when available)
- Regulatory database entries
- Third-party testing reports
- Conference presentations
3. Internal Analysis
- Document cross-reference reports
- Discrepancy analysis
- Evidence gap assessments
- Verification status updates
Verification Status Levels
| Status | Description |
|---|---|
| Verified | Independently confirmed by multiple sources |
| Manufacturer-claimed | Stated by manufacturer, not independently verified |
| Not verified | No verification attempted or possible |
| Outdated | Previously verified but evidence is now outdated |
| Conflicting | Sources provide contradictory information |
How to Access
Professional users can request access to specific evidence sources through:
- Technical documentation request form
- Direct inquiry for research purposes
- Evidence update subscription
Transparency Commitment
We commit to:
- Publishing all evidence limitations transparently
- Documenting and publishing discrepancies
- Updating verification statuses as new evidence emerges
- Providing audit trails for all evidence claims
Local Clinical Problem
Professional users need transparent, auditable access to evidence sources and verification statuses to make informed decisions about Chinese biomedical technology.
Chinese Biomedical Solution Scope
The Evidence Library provides a structured repository with source documents, verification statuses, discrepancy analysis, and audit trails.
Evidence Boundary & Verification Limits
Most evidence sources are manufacturer-provided. Independent verification is limited. All limitations are documented transparently.
Local Implementation Gap
Users should request specific evidence sources and conduct their own independent verification before clinical decisions.
Sources and evidence
All technical parameters are manufacturer-provided unless otherwise stated.
- Manufacturer document Manufacturer-provided information Technical specifications, brochures, and IFU documents provided by the manufacturer (Kunpeng Gene / iFIND).
- Regulatory status Local regulatory status not verified Local regulatory status has not been independently verified for this market.