Ambient clinical documentation
Record where source information came from, provider review, patient choice, corrections, retention rules, known limits, and note history.
DigiTrust helps healthcare organizations connect source evidence, repeatable checks, clinician or accountable human approval, approved use, known limits, and a complete review history across important AI workflows.
Designed to complement—not replace—clinical judgment, privacy, security, compliance, ethics, and existing AI governance.
Healthcare organizations already maintain meaningful controls around patient safety, privacy, clinical authority, quality, research, security, and compliance. As AI enters clinical, administrative, research, and patient-facing workflows, those controls need an operational record that shows how they worked in practice.
DigiTrust preserves the review path. It does not make clinical decisions, replace clinicians, provide legal advice, certify regulatory compliance, or override customer governance.
Record where source information came from, provider review, patient choice, corrections, retention rules, known limits, and note history.
Connect source evidence, eligibility rules, recommendation context, human review, known limits, approval, and a complete decision history.
Record where content and data came from, the approved purpose, personalization rules, human escalation, known limits, and accountability.
Review scheduling, automation, knowledge assistants, data and tool access, approval, exception handling, and review evidence.
Preserve evaluation evidence, success criteria, safety checks, deployment approval, known limits, rollback decisions, and evidence for expansion.
Connect source evidence, AI-system context, checks, clinician approval, recommendation limits, exceptions, and the final accountable decision.
Identify what information, systems, models, tools, and events influenced the AI-assisted result.
Record clear checks for integrity, quality, supporting facts, approval rights, conflicts, and safe disclosure.
Record the reviewer, role, approved purpose, conditions, decision, and time period.
Show whether the AI was used for the approved purpose and stop changed or withdrawn use from inheriting approval.
State uncertainty and unavailable evidence clearly and preserve the history for governance, quality, privacy, security, or later review.
Begin with high-level workflow context and synthetic, de-identified, or customer-approved information. Patient-identifiable data, clinical recordings, credentials, and protected health information remain out of the initial discovery path.
Initial discovery can use high-level workflows, synthetic examples, de-identified context, or approved metadata.
DigiTrust records and supports human approval; it does not replace clinical judgment.
Privacy, security, quality, ethics, legal, and compliance teams retain their responsibilities.
Any later data handling depends on contracts, architecture, access controls, security requirements, and customer authorization.
DigiTrust is publicly listed in AWS Marketplace. For qualified opportunities, DigiTrans can work with the customer and AWS teams to confirm how AWS is involved, the implementation approach, healthcare-specialist participation, purchasing, and production expansion.
AWS Marketplace availability does not imply AWS endorsement or a guarantee of clinical, patient-safety, security, privacy, regulatory, or business outcomes.
Request a 30-minute briefing to identify the strongest workflow, accountable stakeholders, information needed for review, how AWS is involved, and the pilot path.