R0044/2026-04-01/Q001 — Self-Audit¶
ROBIS 4-Domain Audit¶
Domain 1: Eligibility Criteria¶
Rating: Low risk
| Criterion | Assessment |
|---|---|
| Criteria defined before searching | Yes — system-side vs. human-side distinction established before searches |
| Criteria applied consistently | Yes — same distinction applied across all sectors |
| Criteria shift detected | No — criteria remained stable throughout |
Notes: The system-side vs. human-side distinction was clear from the query and applied consistently to all sources.
Domain 2: Search Comprehensiveness¶
Rating: Some concerns
| Criterion | Assessment |
|---|---|
| Multiple search strategies used | Yes — 3 searches across regulatory standards, cross-sector frameworks, and sector-specific guidance |
| Searches designed to test each hypothesis | Yes — searched for both the existence and absence of system-side requirements |
| All results dispositioned | Yes — 60 results returned, all dispositioned |
| Source diversity achieved | Yes — EU legislation, US federal standards, sector-specific regulators |
Notes: Concern: Several key PDFs (NIST AI 600-1, CSET brief, GAO report) were inaccessible for full-text analysis. Secondary sources were used, but full-text analysis might have revealed more specific system-side provisions. Additionally, classified/restricted procurement specifications were not accessible.
Domain 3: Evaluation Consistency¶
Rating: Low risk
| Criterion | Assessment |
|---|---|
| All sources scored using same framework | Yes — reliability, relevance, and bias dimensions applied uniformly |
| Evidence typed consistently | Yes — Factual vs. Analytical typing applied consistently |
| ACH matrix applied | Yes — all evidence mapped to all hypotheses |
| Diagnosticity analysis performed | Yes — most and least diagnostic evidence identified |
Notes: Scoring was consistent across sources regardless of whether they supported or contradicted the researcher's likely expectation.
Domain 4: Synthesis Fairness¶
Rating: Low risk
| Criterion | Assessment |
|---|---|
| All hypotheses given fair hearing | Yes — H1 (enforceable requirements exist) was actively searched for despite the evidence trending toward H2 |
| Contradictory evidence surfaced | Yes — EU AI Act Article 14 was surfaced as the strongest partial exception to the dominant finding |
| Confidence calibrated to evidence | Yes — Medium confidence reflects accessible published frameworks but inaccessible procurement specifications |
| Gaps acknowledged | Yes — classified procurement specs, inaccessible PDFs, and forthcoming EU implementing regulations all documented |
Notes: The finding aligns with what the query framing suggested, but the assessment is supported by evidence from multiple independent regulatory bodies.
Domain 5: Source-Back Verification¶
Rating: Low risk
| Source | Claim in Assessment | Source Actually Says | Match? |
|---|---|---|---|
| SRC02 | Article 14 requires systems be "designed" for automation bias awareness | Article 14 uses "designed and developed in such a way" language targeting providers | Yes |
| SRC04 | FDA relaxed multiple alternatives requirement | Cooley analysis confirms singular recommendations now qualify for enforcement discretion | Yes |
| SRC03 | NIST identifies confabulation as a risk | Secondary sources confirm confabulation is one of 12 identified GenAI-specific risks | Yes |
| SRC05 | FINRA focuses on supervisory procedures | FINRA guidance references Rules 3110/3120 supervisory requirements | Yes |
Discrepancies found: 0
Corrections applied: None needed
Unresolved flags: None
Notes: All claims verified against source content. The limitation is that some verification relied on secondary source analysis (Cooley for FDA, various summaries for NIST) rather than primary document full-text.
Overall Assessment¶
Overall risk of bias: Low risk
The research process was systematic, covering all four target sectors plus cross-sector frameworks. The main limitation is inaccessibility of some primary documents (PDFs) and the inherent limitation that procurement specifications may contain requirements not visible in published regulatory frameworks.
Researcher Bias Check¶
- Confirmation bias risk: The query framing implied the researcher expected a gap in system-side requirements. The evidence confirmed this expectation, raising the risk that the search was optimized to confirm the gap rather than find exceptions. Mitigated by: actively searching for system-side requirements using expanded vocabulary; identifying EU AI Act Article 14 as a partial exception; documenting inaccessible sources that might contain stronger system-side provisions.
- Availability bias risk: Publicly accessible regulatory documents are easier to find than procurement specifications or internal agency guidance. The assessment may underrepresent system-side requirements that exist in less accessible formats.