Never start a
study document from
a blank pageagain.
ReSkript's AI generates a draft of your protocol, ICF, IB, manuscript, abstract,
or final study report that's 90% submission-ready — in two to three hours.
Structured, referenced, and ready for you to review.
The science is the easy part.
The paperwork is where the
weeks go.
Ask any investigator or medical writer where a study document's time
actually goes, and it's rarely the thinking. It'sthe blank page.The
reformatting. Rebuilding the same structural sections study after study.
Chasing references and checking they're cited properly. You need two or three uninterrupted hours to get into the zone — and those hours are the hardest thing to find. So the draft waits. And the timeline slips.
80-100
hrs
to draft a single protocol from scratch
30-40
%
of drafting time recovered —
an 80-hour protocol brought down toward 40–50
80-100
hrs
of uninterrupted focus needed to write well — and rarely available
02
What ReSkript does
One tool. Every document
your study needs.
ReSkript produces a complete draft — every section, 90% ready for submission — and hands it to you as an editable Word file, ready for tracked-change review. You're never editing inside a black box, and never starting from nothing.
Protocols
Study Protocols
All types — interventional, observational,
and investigator-initiated.
Consent
Informed Consent
Plain-language ICFs, structured to standard
and ready to adapt.
Brochure
Investigator's Brochure
Drug background, mechanism, safety, and
preclinical to clinical data.
Publication
Manuscripts
First drafts built directly from your study
results.
Congress
Abstracts
Concise, submission-ready summaries for
scientific congresses.
Reporting
Final Study Reports
Complete end-of-study reporting, drafted
from your results.
03
How it works
From inputs to a working
draft in three steps.
01
Tell ReSkript about your study
Select the document type and enter your study
details — design, indication, endpoints, drug, and
the inputs you already have.
02
Get a near-complete draft in under
two hours
ReSkript drafts every section — rationale to
references — 90% ready for submission and
structured against current standards.
03
Review, revise, and own it
Everything opens in Word. You edit, add your
scientific judgment, and keep full control of the
final version.
A near-final draft in hours. The last 10% is yours.
04
Trust & compliance
Built for documents that
have to hold up.
A first draft is only useful if you can defend it. ReSkript is designed around the standards clinical documents are judged by — and around the reality that the investigator or writer stays accountable for the final work.
Referenced to current standards
Drafts are structured against ICH/GCP and relevant regulatory
guidance, so you start aligned instead of retrofitting.
Citations you can actually check
Every referenced claim links to its source — no vague or
invented citations. You see where each statement came from.
Human oversight, by design
ReSkript produces the draft; you review, revise, and approve.
Accountability for accuracy and compliance stays with you.
Disclosure-ready
AI involvement is transparent and easy to document, in line with
institutional and journal AI-disclosure policies.
05
How complete the draft is
A complete draft — 90%
ready in two to three hours.
ReSkript doesn't hand you a skeleton to finish. In the time it takes to see a few patients, its AI drafts every section of the document — including the scientific rationale, background, eligibility criteria, and endpoints — referenced and structured to standard. What's left is expert review, not writing from scratch.
90%
drafted & referenced — in 2–3 hours
10%
your review & sign-off
Every section, fully drafted
✓
Scientific rationale and background
✓
Study design and procedures
✓
Eligibility criteria
✓
Endpoints and assessments
✓
Statistical considerations
✓
Adverse-event reporting and drug accountability
✓
Regulatory and ethical sections
✓
References — gathered, cited, and formatted
Your final 10%
›
Read the complete draft in Word
›
Apply your clinical and scientific judgment
›
Adjust anything specific to your study
›
Review, revise, and sign off — you stay
accountable
You start from a near-final document, not a blank page — and keep full authorship
of the science that carries your name.
06
Who it's for
Two kinds of writer.
One blank page to remove.
Investigators & independent researchers
Run your own studies without the paperwork stealing your time.
If you're a clinician running investigator-initiated research, the
bottleneck isn't the idea — it's finding protected time to write
while seeing patients. Protocols wait. Manuscripts wait. Studies
stall.
ReSkript gives you a complete first draft to work from in an
afternoon, not weeks — so a study idea becomes a submittable
document while the momentum is still there. You reclaim focus
hours you never had, and stay in full control of the science that
carries your name.
Works for a single study or across an institution's
investigators — ask us about site and Clinical Trials Office
licensing.
Medical writers · pharma, biotech, CRO
Spend your time on the writing that matters — not the blank page.
The value isn't in retyping the same structural sections or
wrestling a document into shape from nothing. It's in the
science, the accuracy, and the review.
Start from a structured draft, not scratch
— cut an estimated 30–40% of drafting time on every document.
QC built in
— automated checks for consistency, numbers, and compliance, like a second reviewer inside the tool.
Citations done right
— proper, source-linked references that solve the citation problems generic AI leaves behind.
You stay the author
— every draft is yours to edit, refine, and sign off.
Fewer review cycles. Better margins on fixed-fee work.
07
Security & confidentiality
Your study data stays yours.
Clinical and patient data isn't something you hand over lightly — and you shouldn't have to. ReSkript is built so that using it never means giving up control of your data.
Never used to train models
What you put in stays yours, full stop. Your data is never used to
train anything.
Encrypted in transit and at rest
Standard, serious data protection at every step of the process.
Access controls you manage
You decide who in your team or institution can see what.
Built to fit institutional policy
Designed to align with hospital, university, and sponsor data-
handling and AI requirements.
08
How ReSkript is built
Purpose-built AI,
shaped by people who
write these documents.
ReSkript is powered by advanced AI trained 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 the point: the speed of AI, guided by
people who know what a submission-ready protocol, IB, or
manuscript actually has to contain — and where generic tools
get it wrong.
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.
See what ReSkriptactually produces.
The best way to judge a first draft is to read one. See a real,
structured, fully referenced draft — and decide for yourself.
