Assessment workflow
This page describes how to complete a defensible GTSAF assessment from preparation through final assurance reporting.
Before starting
Section titled “Before starting”Confirm that:
- The correct workspace is open.
- The AI system is registered.
- The intake record describes the current use case and architecture.
- The system owner and assessment owner are identified.
- The linked System Record and Intake contain complete, conflict-free routing facts.
- ACRS has been reviewed where its additional depth is material to the assessment.
- The intended assessment boundary is documented.
- The assessment is in edit mode and not locked.
- The assessor has access to the required evidence, testing and findings modules.
Step 1: define the assessment boundary
Section titled “Step 1: define the assessment boundary”Record:
- The named AI system and system reference.
- Business purpose and intended use.
- Users and affected people.
- Deployment model.
- Models and providers.
- Data categories and sources.
- Interfaces, APIs and integrations.
- RAG, prompts, context stores and retrieval sources.
- Agentic tools, memory and delegated actions.
- Human decision points.
- Environments in scope.
- Jurisdictions and regulatory roles.
- Suppliers and shared-responsibility boundaries.
- Known exclusions.
Avoid boundaries such as “the AI platform” without naming the actual components and operating relationships.
Step 2: select the GTSAF scope
Section titled “Step 2: select the GTSAF scope”Choose:
- All GTSAF controls
- AI system: authoritative intake route complete
For a formal multi-system assessment, select the named system. ACRS confirmation is not required to determine factual applicability; where ACRS is unavailable, the screen identifies that no confirmed ACRS depth overlay is being used.
Review:
- Applicable-control count.
- Baseline, Triggered and Enhanced depth counts.
- Depth-weighted workload and assurance intensity.
- Factual scope drivers and their overlap warning.
- Applicability-pending controls.
- Out-of-scope controls.
- The reason shown for each control’s applicability.
Confirm that:
Baseline + Triggered + Enhanced = Applicable controls
and:
Applicable controls + Applicability pending + Out of scope = 358
Do not interpret the largest applicable-control count as the highest-risk system. Applicable count measures breadth; workload and assurance intensity explain required rigour. If professional judgement identifies an additional relevant control, include and assess it without changing the underlying Intake merely to obtain a preferred count.
Step 3: work domain by domain
Section titled “Step 3: work domain by domain”GTSAF is organised A to Q. A practical assessment sequence is:
- A-C: governance, legal and intake.
- D-G: data and model engineering.
- H-I: prompt, retrieval, inference and runtime.
- J-L: identity, agentic action and supply chain.
- M-N: monitoring, oversight and impact.
- O-Q: resilience, assurance and infrastructure.
This order establishes governance and system facts before detailed technical testing.
Step 4: read the full control advisory
Section titled “Step 4: read the full control advisory”For each control, review:
- Control statement.
- Objective.
- Risk addressed.
- Applicability explanation.
- Criticality.
- Gate status.
- Implementation guidance.
- Required evidence.
- Test procedure.
- Control owner.
- Evidence owner.
- Cross-framework mappings.
- Role-specific guidance.
Do not assess from the short title alone.
Step 5: answer each assessment question
Section titled “Step 5: answer each assessment question”Select Yes only when the requirement is met in the selected scope.
A Yes answer should be accompanied by:
- Clear implementation narrative.
- Named responsibility.
- Relevant evidence.
- Testing where operating effectiveness matters.
Yes is an assessor claim, not proof by itself.
Select No when the requirement is absent, incomplete or ineffective.
Then:
- Explain the precise deficiency.
- Identify the risk or consequence.
- Link or raise a finding.
- Record compensating controls.
- Assign remediation.
- Decide whether deployment restrictions or escalation are needed.
No creates a Gap. On a Gate control it creates a Gate fail.
Select N/A only where the requirement genuinely does not apply to the selected boundary.
Complete:
- Detailed rationale.
- Decision category.
- Decision owner.
- Independent approver.
- Approval date.
- Review date or reassessment trigger.
- Evidence references.
- Compensating controls or boundary safeguards.
Until the governance fields are complete, the N/A is not honoured.
Step 6: assign shared-responsibility ownership
Section titled “Step 6: assign shared-responsibility ownership”Choose the party that actually operates or assures the requirement:
- MP
- OSP
- AP
- AIC
- CSP
- Shared
- ND
For Shared:
- Identify which party performs each activity.
- Identify which party remains accountable.
- Link contractual or architectural evidence.
- Explain how gaps and incidents are escalated across the boundary.
Resolve ND before sign-off.
Step 7: document implementation
Section titled “Step 7: document implementation”The implementation narrative should state:
- What is implemented.
- Where it is implemented.
- Who operates it.
- Which systems or environments it covers.
- How often it operates.
- How exceptions are handled.
- How changes are approved.
- Which evidence demonstrates operation.
- What the customer or another provider must do.
- Known limitations.
Avoid statements such as:
- “Industry best practice is followed.”
- “The vendor handles this.”
- “Security is enabled.”
- “Compliant.”
Those statements are not testable without further detail.
Step 8: collect and link evidence
Section titled “Step 8: collect and link evidence”Use the control’s Required evidence advisory as the starting checklist.
For each artefact:
- Link it to the correct control.
- Link it to the correct system or intake.
- Record owner and date.
- Review its relevance, sufficiency and currency.
- Record the review status.
- Record evidence quality.
- Reject generic or stale material.
Narrative does not become verified evidence through keyword matching.
Step 9: perform control testing
Section titled “Step 9: perform control testing”Use the control-specific test procedure to design a bounded test.
Record:
- Test objective.
- Test steps.
- Population and sample.
- Expected result.
- Pass criteria.
- Safety limits.
- Test date.
- Tester.
- Result.
- Exceptions.
- Retest date.
Do not conduct destructive production tests without explicit authorisation.
Step 10: raise findings
Section titled “Step 10: raise findings”Raise a finding when:
- A question is No.
- A Gate fails.
- Evidence is rejected or materially insufficient.
- A test fails or produces an exception.
- Ownership is unresolved.
- The implementation differs from policy or contract.
- The control cannot be demonstrated in operation.
- A Critical control lacks required test coverage.
A useful finding contains:
- Clear title.
- Affected control and system.
- Condition observed.
- Expected requirement.
- Evidence.
- Root cause.
- Risk consequence.
- Severity.
- Recommendation.
- Owner.
- Target date.
- Status.
Step 11: record the assessor conclusion
Section titled “Step 11: record the assessor conclusion”Complete the structured conclusion:
- Design effectiveness.
- Implementation effectiveness.
- Operating effectiveness.
- Evidence conclusion.
- Residual risk.
- Assessor conclusion.
- Monitoring cadence.
- Reassessment triggers.
- Reviewer.
- Review date.
The conclusion should identify:
- What was reviewed.
- What was tested.
- What could not be verified.
- Open exceptions.
- Compensating controls.
- The basis for residual risk.
- The conditions under which the conclusion expires.
Step 12: review the derived result
Section titled “Step 12: review the derived result”Review:
- Conformance.
- Verified evidence.
- Narrative sufficiency.
- Ownership clarity.
- Audit readiness.
- Assurance percentage.
- Assurance score.
- Gate failures.
- Critical-control evidence and tests.
- Open findings.
Do not use the headline score without reading the underlying gaps and caps.
Step 13: use AI Assist
Section titled “Step 13: use AI Assist”AI Assist can:
- Summarise the current validated scope.
- Identify evidence and testing gaps.
- Suggest bounded test procedures.
- Draft effectiveness and residual-risk reasoning.
- Identify monitoring and reassessment needs.
The assessor must:
- Confirm the displayed system scope.
- Check every claimed verified fact.
- Reject invented or unsupported conclusions.
- Decide whether to apply suggestions.
- Retain human accountability.
Step 14: perform quality review
Section titled “Step 14: perform quality review”Before sign-off, ask:
- Is the correct system selected?
- Is the authoritative Intake route complete and current?
- Has ACRS been reviewed where it changes required assurance depth?
- Do the scope and depth totals reconcile?
- Can the factual scope drivers be explained?
- Are all Mandatory, Triggered and Enhanced controls addressed?
- Are Critical and Gate controls prioritised?
- Are N/A decisions independently approved?
- Are Yes answers supported by linked evidence?
- Are Critical controls tested?
- Are failed tests and rejected evidence reflected in the conclusion?
- Are all findings linked and owned?
- Does residual risk reflect open exceptions?
- Are monitoring and reassessment triggers specific?
- Does the report use the correct system bucket?
Step 15: lock and report
Section titled “Step 15: lock and report”Once reviewed:
- Lock the assessment according to your governance process.
- Generate the appropriate system or workspace report.
- Obtain formal review or approval.
- Record risk acceptance separately where required.
- Schedule the next review.
Locking prevents assessment changes and AI suggestions from being applied without reopening the governed workflow.
When reassessment is required
Section titled “When reassessment is required”Reassess after:
- A new model or major model version.
- New training data or a changed retrieval corpus.
- A supplier or hosting change.
- New tools, plugins, memory or autonomy.
- Expanded privileges or system access.
- New personal or sensitive data.
- A move into a new jurisdiction.
- A serious incident, complaint or control failure.
- A material change in intended use.
- A failed control test.
- A regulatory or contractual change.
- Expiry of a N/A decision or evidence item.
Minimum sign-off record
Section titled “Minimum sign-off record”A defensible sign-off should include:
- System and scope.
- Assessment date.
- Assessor and reviewer.
- Applicable control population.
- Gate failures.
- Critical control status.
- Evidence and testing summary.
- Open findings.
- Residual risk.
- Deployment or use restrictions.
- Monitoring cadence.
- Reassessment triggers.
- Approval decision.