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Health & science
Keep research, quality, and supplier documents connected to their review history.
Life-sciences teams work with carefully controlled document versions. Signed evidence can help reviewers identify what was submitted and approved alongside the organization’s validated operating systems.
A review package may contain several revisions of specifications and test reports.
Record the package manifest, document fingerprints, controlled version references, and the responsible review event.
Compare the package used in follow-up work with the recorded version and handle changes through your quality system.
An additional evidence link between a document set and its recorded review.
Analysis files move between teams without a consistent description of their source version.
Create a signed manifest of approved dataset references, file fingerprints, method version, and the transferring team’s identity.
Check the received package and evaluate the research methods and data quality through the established scientific review.
A traceable research handoff with a defined set of files and methods.
Procurement and quality staff may review different copies of a supplier’s certificate.
Record the certificate fingerprint, supplier source, referenced batch or product, and the assessment outcome.
Check the presented version and verify the supplier’s claims through the organization’s approved assurance procedures.
A shared reference for the supplier evidence the team assessed.
Put it into practice
Start with the capability your first use case needs. Add others as your process grows.
Turn a credential, approval, or statement into a digitally signed record with an identifiable issuer.
Package a record’s signature and supporting verification information for inspection outside the original application.
Manage access, signing identities, policies, and audit records from a shared organizational workspace.
Evaluate validation, retention, data, and signature requirements before integration. Truthlocks records support your evidence process and do not independently establish regulated-system compliance.
Use cases describe how to apply the platform. Your workflow may need APIs, external systems, and configuration; available features depend on your plan.
Explore documents & approvalsKeep exploring
Organize staff credentials, supplier evidence, and administrative review records.
Add traceable source, release, and administrative action records to health applications.
Connect datasets, laboratory reports, and research deliverables to recorded sources.