A WCAG 2.2 AA audit of your patient portal. Run under PHI-aware doctrine.
Four to six weeks. BAA before any access. Findings calibrated to OCR enforcement themes — Section 1557, the 2024 HHS web accessibility rule, ADA Title II / III. Designed for portals under enforcement scrutiny, EHR-integration releases, and payer-portal procurement deadlines.
$35,000–$55,000 Four to six weeks · T&M with cap · BAA before access
A schematic of a patient-portal surface — login, dashboard, lab results, secure messaging, scheduling — with a translucent PHI-handling ribbon threading through the audit pipeline (evidence capture, recording storage, transcript review, deliverable). Reads as "the WCAG audit that respects what the surface actually carries." Architectural, not clinical. No stethoscopes, no stock-doctor imagery.Patient portals are where a11y findings, PHI handling, and OCR enforcement collide.
A patient portal landed an OCR complaint. Or your health system is releasing a new MyChart-shape surface, or migrating off one. Or a payer portal RFP just asked for your accessibility posture and the deadline is real. The surface in question carries protected health information, serves cohorts with vision, motor, cognitive, and auditory impairments at higher base rates than the general population, and is governed by an enforcement regime — Section 1557 effective communication, the 2024 HHS web accessibility rule, ADA Title II / III, and OCR investigative authority — that is more aggressive than the procurement context most a11y firms are calibrated to.
The market response is uneven. Generic a11y firms run an axe-core dump and refuse to touch PHI; some will not sign a BAA at all. Some healthcare consultancies will sign the BAA but their accessibility methodology is shallow — interviews, not engineering judgment, no component file:line citation. Either way, the artifact you receive is not the artifact your privacy officer, patient-experience lead, and counsel can all act on at the same time.
G1 is the patient-portal a11y audit run from healthcare-credentialed engineering doctrine. The same operator who built HELiX — our open-source healthcare component library shipping at WCAG 2.1 AA — leads the audit. The BAA is countersigned through Clarity House LLC before any access. Recordings are captured, redacted, and stored under PHI-aware engineering controls. Findings cite WCAG 2.2 SC, component file:line, and where the fix touches a HIPAA-sensitive flow. The executive summary is calibrated to OCR enforcement themes. The deliverable is one report your privacy officer, patient-experience lead, engineering team, and counsel can act on without a translation pass.
What you get
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WCAG 2.2 AA findings — patient-portal calibrated
Findings cite the specific WCAG 2.2 success criterion, the page or template, the element, and (where the consumer is built on a known component library) the component file:line. Calibrated to the surfaces patient cohorts actually use — login, dashboard, lab results, secure messaging, scheduling, telehealth entry — and to the OCR enforcement themes attached to those surfaces.
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Severity-rated remediation roadmap
Findings ranked by severity (blocker / serious / moderate / cosmetic), ordered for sequenced remediation, sized in engineering effort, and tagged where the fix touches a HIPAA-sensitive flow versus a non-PHI flow. Slottable into a sprint without a translation pass.
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PHI-aware assistive-tech matrix evidence
Screen-reader, keyboard-only, zoom, and (where in scope) speech-input evidence captured against the patient-portal surface. NVDA / JAWS / VoiceOver / TalkBack as scoped. Recordings captured, redacted, and stored under PHI-aware engineering controls — per-recording consent, PHI scrub on persistence, encrypted at rest, accessible only to the engagement principal and BST internal counsel.
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Executive summary — OCR-calibrated
One page, plain language, calibrated to the OCR enforcement themes attached to patient-facing surfaces — Section 1557 effective communication framing, ADA Title II / III where applicable, and the 2024 HHS web accessibility rule for covered entities. Counsel-readable, board-readable, privacy-officer-readable.
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Signed audit report
Signed under principal-engineer attestation through Clarity House LLC. The artifact your counterparty receives. Note: this is principal-engineer attestation, not the regulatory third-party-assessor designation; we will tell you up front when your enforcement context requires the latter.
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90-minute findings walkthrough
Engineering, design, patient-experience lead, privacy officer, and (where present) counsel attend; we walk every finding with the BST principal who did the work. Questions answered, follow-up scope identified, BAA chain implications surfaced.
How it works
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BAA & Access
Week 1Deliverable Executed BAA, access provisioned under PHI-aware engineering controls
Business Associate Agreement executed through Clarity House LLC before any PHI access. Engagement environment stood up — encrypted recording storage, PHI scrub on persistence, per-recording consent capture for assistive-tech matrix evidence, audit-log retention. Scope locked: surfaces in audit boundary, EHR integration scope, locale coverage, AI-mediated features in scope. We do not begin technical work until the BAA is countersigned and the engagement environment is verified.
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Audit pass
Weeks 2–3Deliverable WCAG 2.2 AA findings against the scoped patient-portal surface
Every page or template walked against WCAG 2.2 AA, with assistive-tech evidence captured under PHI-aware doctrine. axe-core and Pa11y are part of the toolchain; they are not the audit. The audit is engineering judgment applied to a patient-facing surface, with OCR enforcement themes and HIPAA-sensitive-flow tagging running in parallel.
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Severity & roadmap
Weeks 3–4Deliverable Severity-rated findings, remediation roadmap, executive summary draft
Findings rated and sequenced. Roadmap drafted with engineering effort sized per finding and PHI-touching flows tagged. Executive summary calibrated to OCR enforcement themes — Section 1557 effective communication, the 2024 HHS web accessibility rule, ADA Title II / III as applicable. Internal QA pass before the report goes out.
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Walkthrough & delivery
Weeks 4–6Deliverable Walkthrough call + signed report + evidence destruction certificate
Walkthrough with engineering, design, patient-experience lead, privacy officer, and (where present) counsel. Revisions incorporated. Signed report delivered under principal-engineer attestation. Recorded evidence destroyed per BAA / engagement protocols, with destruction certificate provided.
Pricing
Engagement model Time & materials with not-to-exceed cap
Compact tier (single patient-portal surface, single locale, single integration boundary, single BAA in scope) lands at $35K–$42K / 4 weeks. Standard tier (multi-flow portal — dashboard, lab results, secure messaging, scheduling — with EHR integration in the audit boundary) lands at $42K–$48K / 4–5 weeks. Complex tier (multi-locale portal, telehealth surface in scope, or AI-mediated feature on the portal — e.g. visit-note summarization or symptom-checker — folded into the audit) lands at $48K–$55K / 5–6 weeks. Time-and-materials with a not-to-exceed cap. PHI-aware engagement controls — BAA execution, encrypted recording storage, PHI scrub on persistence, per-recording consent capture, evidence destruction certificate at close — are included in the cap, not an add-on line item.
Anchor pricing reflects typical engagement ranges. Actual fees are scoped per engagement under time-and-materials with a not-to-exceed cap. Pricing shown does not constitute a binding offer.
Frequently asked questions
How long does this take?
What does this cost?
- Compact tier: $35K–$42K (single portal surface, single BAA)
- Standard tier: $42K–$48K (multi-flow portal, EHR integration in scope)
- Complex tier: $48K–$55K (multi-locale, telehealth, or AI-mediated feature)
Do you sign a BAA?
How is this different from A1?
- BAA executed before access
- Encrypted recording storage with PHI scrub on persistence
- Per-recording consent for assistive-tech matrix evidence
- Evidence destruction certificate at close
How is this different from a Healthcare AI Compliance Review?
Will the report stand up under counsel and OCR scrutiny?
What if you find a reportable breach indicator while auditing?
Will you do the remediation work too?
What if the portal embeds an AI feature — visit-note summary, symptom checker?
Are you a third-party assessor?
Often combined with
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Healthcare AI Compliance Review
Every patient-portal surface is also a HIPAA surface. WCAG audit here, HIPAA / BAA chain / SaMD lens there. Common attach when the same release window needs both signatures; PHI-aware engagement infrastructure is shared.
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Single Property Accessibility Audit (A1)
When the patient portal is part of a larger property family — marketing site, public-facing scheduler, member portal — A1 covers the non-PHI surfaces and G1 covers the patient-portal surface. Two engagements, calibrated scopes, single buying motion.
Ready to audit the portal under doctrine that respects what it carries?
Four to six weeks. BAA before any access. Findings calibrated to OCR enforcement themes. Signed under principal-engineer attestation.