ReSkript for Medical Writers

ReSkript's AI drafts protocols, ICFs, IBs, manuscripts and abstracts to 90% submission-ready —
cutting 30–40% of your drafting time. With QC and source-linked citations built in.

Where the real value is

"The real value would be inreducing the blank-page effort —instead of starting from scratch."

The value isn't retyping the same structural sections — it's the science, the accuracy, and the review.
A strong, structured draft from your existing data saves time before you write a word.
It's not just more projects — it's better margins on fixed-fee work and fewer review cycles.
Less time on repetitive drafting means more time on the parts that need a human.

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Built around what you actually asked for

Everything a first draft shouldbe — and everything generic AI isn't.

ReSkript was shaped with medical writers, around the things that decide whether a tool is worth buying: accuracy, citations, QC, and control.

Start from a structured draft, not scratch

Reduce the blank-page effort on every document. A complete, 90%submission-ready draft — rationale to references — in two to threehours.

QC built in

Automated checks for consistency, numbers, and compliance —almost like a second reviewer built into the tool, reducing the back-and-forth during reviews.

Citations done right

Proper, source-linked references with clickable links — solving ‍the citation problems generic AI leaves behind. Every claim you can check.

You stay the author

Every draft is an editable Word file, tracked-change ready. You review, revise, and sign off — accountability stays with you.

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What you can draft

Every document type in yourworkload — one tool.

Protocols across every study type, plus ICFs, IBs, manuscripts, abstracts, and final study reports — tailored to the design and to FDA or EMA context.

Observational

> Case, case-control & case series
> Cohort (pro / retrospective)
> Cross-sectional
> Population studies

Interventional — drug

> Phase I, II, III
> Phase I/II, II/III
> Adaptive, all phases
> FDA & EMA variants

Interventional — device

> Phase I
> Phase II
> Phase III — class I
> Phase III — class II & III

Specialised

> Behavioral
> Bioequivalence
> Therapeutic equivalence
> Bioavailability

Beyond the protocol

> Informed Consent Forms
> Investigator's Brochures
> Manuscripts & publications
> Congress abstracts

End of study

> Final study reports
> Drafted from results
> Structured to standard
> Ready for review

How ReSkript is built

Purpose-built AI, shaped bymedical writers.

ReSkript is powered by AI built for clinical and scientific documentation — not a general chatbot. It was developed by MphaR together with medical writers from pharma, biotech, and CROs, and independent researchers, with decades of experience producing these exact documents. That's why it handles citations, consistency, and compliance the way generic tools don't.

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