ReSkript Trust

ReSkript is designed for documents that have to hold up, and for people who cannot afford to hand their data anywhere. Here's exactly how your data is handled, where every reference comes from, and who built the tool.

Data security

Your data goes nowhere. It's analysed, then deleted.

Investigators and medical writers work with some of the most sensitive information there is — study data, patient details, unpublished results, confidential sponsor materials. ReSkript does not pass that data anywhere. It is used solely to produce your document inside ReSkript, and once the analysis is complete, it is deleted.

Analysed inside ReSkript. Deleted after.

The data you provide is used only for the analysis that generates your draft — nothing else. It is never shared, never sold, and never used to train any model. As soon as the analysis is done, your data is deleted.

You provide inputs

Study details and the materials you already have, entered securely.

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Analysed inside ReSkript

Used only to generate your document — never passed to any third party.

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Deleted after analysis

Once your draft is produced, the data you provided is deleted.

No third parties · no model training on your data · deleted after analysis

Access controls you manage

You decide who can see your documents. Whether you work independently or in an institutional team, access stays under your control.

You keep the output

Every draft is delivered as an editable Word file that belongs to you. No lock-in — take it, edit it, and store it wherever your workflow requires.

Encrypted in transit and at rest

For the time your data is being processed, it is protected with strong encryption — while it travels to ReSkript and while it is held for analysis.

Never used to train AI

What you put in is used to help you — not to improve ReSkript's models or anyone else's. Your data never becomes training data.

Deleted once analysed

ReSkript retains your data only for as long as it takes to generate your draft. When the analysis is complete, the data is deleted — it is not stored indefinitely.

Never passed to third parties

Your inputs stay within ReSkript for the sole purpose of producing your document. They are not shared or handed to any outside party.

Referenced & cited

Every claim referenced — only from trusted, published sources.

Generic AI invents citations, or references things that don't exist. ReSkript doesn't. Every referenced statement is drawn only from trusted, peer-reviewed and official published sources — and each citation is real, source-linked, and yours to verify.

Eligibility criteria are defined in accordance with Good Clinical Practice requirements ↗ CH E6(R3) · §4.3 and reflect the recommended safety monitoring intervals for this class of ↗ agent source [12] .

Sample size is justified using the effect estimate reported in the pivotal published trial ↗ source [7] ↗ linked , with assumptions documented for review.

Every source is real and clickable — verify each reference against its origin. No invented or mismatched citations.

Compliance

A secure, compliant platform.

Developed in collaboration with healthcare professionals and pharmaceutical companies, ReSkript is designed to ensure security and compliance at every stage. Built as a HIPAA-compliant, cloud-based solution, it adheres to ISO/IEC 27001 and AICPA SOC 2 (TSP Section 100) standards.

HIPAA-compliant

Handling of protected health information to US healthcare standards.

ISO/IEC 27001

Internationally recognised information-security management standard.

AICPA SOC 2

Trust Services Criteria (TSP Section 100) for security and confidentiality.

Beyond certification, ReSkript is built around the standards clinical documents are judged by — and around the reality that the investigator or writer stays accountable for the final work.

Disclosure-ready

AI involvement is transparent and easy to document, in line with institutional and journal AI-disclosure policies.

Human oversight, by design

ReSkript produces the draft; you review, revise, and approve. Accountability for accuracy and compliance stays with you.

Fits institutional policy

Designed to align with the data-handling and AI-use requirements of hospitals, universities, and sponsors.

QC built in

Automated checks for consistency, numbers, and compliance — like a second reviewer built into the tool.

Referenced to current standards

Drafts are structured against ICH/GCP and relevant regulatory guidance, so you start aligned instead of retrofitting.

FDA & EMA context

Documents can be tailored to FDA or EMA requirements, reflecting the framework your study falls under.

How ReSkript is built

Purpose-built AI, shaped by people who write these documents.

ReSkript is powered by AI built for clinical and scientific documentation — not a general chatbot pointed at a protocol. It was developed by MphaR together with medical writers and independent researchers who have spent decades producing the exact documents ReSkript drafts. That combination is why it handles citations, consistency, and compliance the way generic tools don't.

AI-powered

Advanced language AI, purpose-built for clinical and scientific documents and referenced against current standards.

Built with medical writers

Shaped by professional writers from pharma, biotech, and CROs who produce these documents every day.

Guided by researchers

Informed by independent investigators with decades of experience running and writing their own studies.

An MphaR product

From a specialist Medical Affairs consultancy — Solutions in Medical Affairs.

Common questions

Straight answers on data and trust.

What happens to the data I enter?

It is used only to generate your document inside ReSkript. It is never passed to any third party, and once the analysis is complete, it is deleted.

Is my data stored long-term?

No. ReSkript keeps your data only for as long as it takes to produce your draft. After analysis, it is deleted — not retained.

Is my data used to train the AI?

Never. Your inputs are used to help you produce your document, not to train ReSkript's models or anyone else's.

Where do the citations come from?

Only from trusted, published sources — peer-reviewed literature, ICH/GCP guidance, FDA and EMA publications, and established clinical databases. Every citation is real and source-linked, so you can verify it.

Can I disclose that AI was used?

Yes. AI involvement is transparent and easy to document, so you can meet institutional and journal disclosure requirements.

Who is accountable for the final document?

You are. ReSkript produces the draft; the investigator or writer reviews, revises, and signs off. The tool never takes the decision out of your hands.