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Terms of Use

Last updated 12 July 2026 — pilot phase

This is a working draft, published as part of Clin A Head's pilot phase. It has not yet been reviewed by qualified legal counsel and should be treated as a starting point, not a finished legal instrument, until it has.

1. What Clin A Head is

Clin A Head is a consultation-preparation tool for clinicians. It imports documents a doctor already holds for a patient, produces a structured synthesis, generates a pre-consultation questionnaire, and answers questions about the file in natural language — with every extracted fact traced back to the exact document and line it came from.

2. What Clin A Head is not — and who is responsible for what

Clin A Head does not diagnose, does not prescribe, and does not make clinical decisions. It searches, organises, and restates information already present in a patient's documents. It is not a medical device, is not a substitute for clinical judgement, and must never be treated as one.

3. Intellectual property

Clin A Head — the name, the underlying software, its interface, its documentation, and all associated materials — is the intellectual property of ClinAHead. Nothing in these terms transfers ownership of any part of the software, its source code, its models, or its branding to a user.

4. Data handling

A precise, technical explanation of exactly what is sent for AI processing — and what is deliberately kept back — is published on the main site under Your data. That page is the authoritative description of current data handling; this section summarises the commitments behind it.

5. The pilot programme

6. Availability and changes

Clin A Head is under active development. Features, interfaces, and these terms may change during the pilot phase; participants will be notified of material changes. The desktop application requires a working connection for AI-assisted features (synthesis, chatbot, questionnaire generation); document import and manual review remain available without one.

7. Governing regions

Clin A Head operates with practices in France, the United Kingdom, and Australia. Where local law imposes stricter requirements than stated here — including around health data, medical device regulation, or professional confidentiality — the stricter local requirement governs.

8. Contact

Questions about these terms, the pilot programme, or a specific data-handling question: elyas.sierra@sciencespo.fr.