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AI FOR CLINICAL RESEARCH

Clinical research & professional collaboration

Keep each research record tied to its study, visit and form version so reviewers can return to individual fields and address issues. We build software for collection, revision, role-based review and export. The research team confirms data meanings and acceptance criteria.

RT Clinica product interface: synthetic study and identity data; no real patient information
1

Tasks, operations & human judgment

RT Clinica live-product practice

Collect and revise a research form

Inputs
A fixed form version, field definitions and synthetic example data.
Software actions
Enter records while retaining field status, revision reasons and versions.
Outputs
Forms and revision records within their study and visit context.
Human judgment
Researchers check meanings, add missing information or explain why a field is not applicable.
RT Clinica live-product practice

Resolve review issues and export

Inputs
Records awaiting review, issue labels and role scope.
Software actions
Resolve issues according to roles and export within the agreed scope.
Outputs
Review status and data that preserve field meanings.
Human judgment
Specialists check issue resolution, dates and form versions.
2

Conditions needed to start

Clarify the conditions first.

01

Purpose & participating roles

The research or collaboration task to support, each role's permitted actions and review responsibilities.

02

Fields & form information

Authorized form definitions, field meanings, version rules and example data. Use de-identified or synthetic information during discussions.

03

Access & data conditions

Authorization to use information, data scope, existing systems and export requirements. Sensitive information is handled through methods agreed by both parties.

04

Checking rules

Methods for checking field meanings, revision records, permission boundaries and export results.

3

Which tasks software handles

Choose tools and workflows for the task.

Specific capabilities and operating environments are agreed at the start of each project.

01

Research data collection

Organize entry around studies, sites, visits and fixed form versions, preserving distinctions between missing, not applicable and zero values.

02

Role-based review

Show records, issues and revision reasons within the agreed scope, allowing reviewers to move from a summary to individual fields.

03

Controlled exports & versions

Export according to permissions, retaining original issue labels, actual visit dates and form versions. Isolated tests check access and export meanings.

4

Current project evidence

See what has been built.

RT Clinica is live. Its public case documents research data collection, role-based review, form versions and controlled export. Case summaries, medical Q&A or other AI-assisted functions require separate development and validation for specific tasks.

5

Delivery & acceptance

Task & data boundaries

The task, participating roles, authorization conditions and information scope.

Collection & review workflows

Agreed fields, forms and operating workflows, with example data.

Role & export design

Access rules for each role, revision records and export meanings.

Software checks & handover documentation

Isolated test records, known limitations and usage instructions.

How results are checked

Use isolated environments and de-identified or synthetic data to check collection, review, versions, exports and rejection of unauthorized actions. Software acceptance is handled separately from clinical effectiveness, qualifications or certification.

Professional responsibilities

We build collection, role-based actions and export workflows. The research team is responsible for field definitions, revision reasons and specialist review. Software checks do not replace clinical judgment, clinical effectiveness evaluation or certification.

Validation scope & next-step conditions

For clinical research and professional collaboration; no online diagnosis or treatment advice is provided. Applications involving clinical judgment require corresponding clinical validation, specialist review and applicable approvals. Do not submit patient information through this site.