Trigger: AI is used with research data or participant records.

Research AI Evidence Passport

Make research AI
reproducible, bounded, and reviewable.

Track datasets, models, lineage, consent boundaries, analysis pipelines, RAG systems, and AI agents used in research without turning evidence into bureaucracy.

Dataset lineage & provenanceConsent boundary evidenceReproducibility ReceiptsScientific validity not claimed
Research Data ContextCleared with Limits
Consent scopeEthics reviewed
Model registry traceActive
Dataset version fingerprintCurrent
Cross-institutional DTAConfirmed
PrivacyLineageFairness

Reproducibility Evidence

Model registry trace active
Dataset version fingerprint active
Environment pinned
Consent boundary confirmed

Sensitive context

Why research AI needs evidence infrastructure.

Research AI operates on participant data, proprietary datasets, and models whose outputs may form the basis of published findings. Reproducibility failures, consent boundary violations, and undocumented data provenance undermine scientific integrity and carry legal, ethical, and institutional consequences.

Data categories in scope

Research participant data and responses
Clinical trial or health study data
Proprietary training datasets
Published and pre-publication findings
Cross-institutional shared data

People affected

Research participantsPatients in clinical studiesResearch collaborators and institutionsJournal reviewers and academic communityFunding bodies and ethics committees

Risk scenarios

What typically goes wrong.

Specific failure modes seen in this sensitive context — without structured evidence.

A research model is trained on participant survey data beyond the original consent scope.

Ethics committee requires evidence of consent boundary. No structured evidence exists. Publication delayed or retracted.

An analysis pipeline produces outputs that cannot be reproduced by a reviewer.

No Model Registry Trace active. No dataset version fingerprint. Environment not captured. Reproducibility claim in publication unsupportable.

A research RAG assistant is built over pre-publication manuscripts and raw interview transcripts.

No document boundary. Pre-publication content accessible via queries. Confidential data at risk. No Retrieval Grounding Evidence.

A research AI agent writes portions of a literature review without disclosure.

No provenance tracking. No disclosure mechanism. Institutional integrity policy potentially violated.

Scope

What needs a Passport.

Research analysis AI models and pipelines
Participant data processing AI tools
Literature review and research RAG assistants
Hypothesis generation and discovery AI
Clinical trial data analysis models
Cross-institutional research AI platforms
AI agents used in research workflows

Stakeholder workflow

From trigger to access decision.

1

Trigger

AI system in scope

2

Evidence Request

Passport initiated

3

Review

DPO · CISO · Specialist

4

Decision

Access condition set

5

Monitor

Tide sweeps · Renewal

Principal Investigator

Research AI will process participant data or produce publishable outputs.

Require Passport documenting consent scope, lineage, and reproducibility evidence before deployment.

Ethics Committee / IRB

AI tools are used with participant data in a research study.

Review Passport consent boundary section. Confirm alignment with study protocol.

Data Steward / DPO

Research data shared cross-institutionally via AI platform.

Confirm DTA status, data transfer evidence, and privacy section before cross-institutional access.

Access decisions

Context Visa conditions.

The access decisions that apply in this sensitive context — and the evidence conditions that produce them.

Cleared with Limits
  • Consent scope confirmed and documented in Passport
  • Dataset lineage and versioning active
  • Cross-institutional DTA confirmed
  • Reproducibility evidence: Model Registry Trace active
Review Needed
  • Consent scope unclear or broader than original purpose
  • Lineage absent — cannot reproduce pipeline outputs
  • Cross-institutional transfer without DTA
Human Review Required
  • AI used to generate or draft publication content
  • Research participant data in scope — ethics committee review required
  • Clinical data — IRB / ethics approval confirmation needed
Blocked
  • Participant data processed beyond consent scope
  • Raw unpublished data accessible via uncontrolled retrieval
  • No lineage — publication reproducibility claim unsupportable

Measurement

Evidence families we can structure.

The measurable evidence categories relevant to this context and the evidence signals they produce.

Dataset Lineage & Versioning

Dataset provenance, version history, and transformation lineage from raw data to model inputs.

Model Tracking

Run tracking, hyperparameter capture, and model versioning enabling reproducibility of published analyses.

Consent & Ethics Boundary

Evidence that data processing stays within the scope of participant consent and ethics committee approval.

RAG Document Boundary

Evidence that retrieval scope covers only authorised documents — pre-publication content excluded where required.

Data Export Integrity

Evidence that cross-institutional data transfers occur only under confirmed data transfer agreements.

Privacy

PII detection and de-identification evidence for participant data before analysis or sharing.

PrivacyRAG GroundingLineage

Honest scope

What remains not assessable.

AffectLog does not overclaim. These items require external expertise, regulatory process, or long-term study.

Scientific validity of research findings

Scientific validity requires peer review, methodology assessment, and domain expertise — not an AI evidence platform.

Instead: Submit findings for peer review. Engage domain experts. AffectLog evidence supports the infrastructure review — not scientific assessment.

Ethics committee approval

Ethics approval is granted by institutional review boards and ethics committees following dedicated review processes.

Instead: Engage your institutional IRB / ethics committee. AffectLog evidence can support the application — not replace it.

Whether AI-generated content meets journal or institutional disclosure standards

Disclosure standards are set by journals, institutions, and professional bodies — outside evidence platform scope.

Instead: Refer to your institution's AI use policy and target journal guidelines.

Example

Sample Passport for this context.

AI Evidence PassportCleared with Limits

ClinicalSynth Analysis Pipeline

Clinical trial data analysis model · Health Research

Evidence76%
Expiry30 Jun 2027
Raw data exportoff
ALP-2026-RES-C4S8

Access conditions

Processing scope limited to consented data categories
Model Registry Trace active — outputs reproducible
Dataset version fingerprint: all training data versioned
Cross-institutional access under confirmed DTA only
No raw participant data in RAG scope
Ethics committee review at 12-month intervals

What we will not overclaim

AffectLog provides technical and operational evidence for research AI. We do not claim scientific validity, ethics approval, or publication standards compliance. We show lineage, consent boundaries, reproducibility evidence, and what review conditions apply.

Common questions

Questions this context raises.

We already have run tracking internally — we don't need an additional evidence layer.

Run tracking captures individual experiment runs. AffectLog structures it into a Passport: consent scope, cross-institutional transfer evidence, RAG document boundaries, and access decisions — making internal tooling accessible to ethics committees, DPOs, and institutional reviewers.

Research is exploratory — we cannot know in advance what data we'll need.

Exploratory scopes can be documented as evidence of breadth and intent. A Passport at research start establishes the consent and data boundaries — updated as scope evolves — rather than reconstructing evidence after publication.

Get started

Make research AI evidence
as rigorous as the research itself.

Map which AI tools are in your research pipeline, establish consent and lineage evidence, and structure reproducibility conditions before your next publication cycle.

AffectLog provides technical and operational evidence. Not scientific validation, ethics approval, or publication standards certification.