Write your clinical study protocol in one hour instead of one week
DocGenius transforms clinical protocol writing with AI that guides you through smart questions. Save valuable time while meeting regulatory standards and ensuring flawless documentation for your studies.
Write my protocol nowA new way to write, with you at the center
DocNexus doesn't write for you: it writes with you.
Protocols that are ICH-GCP compliant without the usual effort
Our AI, an expert in clinical research, guides you through every essential section of your protocol. From scientific rationale to inclusion criteria and statistical analyses, DocGenius structures your document to international standards while tailoring it to the specifics of your study.
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Start NowI have always believed that AI should not replace humans, but empower them. DocNexus puts domain expertise back at the center by helping you structure and challenge your thinking. That is what true augmented intelligence looks like.
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AI-Generated Questions
A complete solution for all your medical documents
Beyond clinical study protocols, DocGenius helps you write study reports, consent forms, synopses, investigator brochures, and regulatory submission files. Our AI adapts to all your documentation needs.
See all possible documentsSmart questions with suggestions to speed up your writing
Save valuable time with context-aware questions paired with answer suggestions based on industry best practices. Our AI anticipates your needs and offers wording tailored to your clinical study.
Try the writing assistantContent perfectly tailored to your clinical context
Our AI automatically adjusts the style, level of detail, and terminology based on your medical specialty, your study phase, and your specific regulatory requirements. The generated protocol faithfully reflects your expertise and the particulars of your research.
Customize my protocolReady-to-use documents with professional formatting
Instantly export your protocol in .docx format with a structure that meets the expectations of ethics committees and regulatory authorities. Dynamic table of contents, automatic numbering, and polished layout save you hours of formatting.
See a sample protocolThree steps to write your protocol
A proven technology that radically transforms document production.
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Sign up in seconds and get instant access to our assistant specialized in clinical study protocols. No credit card required to get started.
Answer the AI's questions
Our AI guides you with targeted questions about your study. Each answer refines the document and structures your protocol according to current standards. Benefit from suggestions based on best practices.
Get your complete protocol
In less than an hour, receive a structured, compliant clinical study protocol ready for submission. Export it to Word with professional formatting, including a table of contents and appendices.
Built-in multilingual support for your international studies
Write and export your protocols in English, French, German, Spanish, Italian, or Portuguese. Ideal for international multicenter studies and for streamlining submissions to foreign regulatory authorities without extra translation work.
Change my protocol's languageSmart regeneration for instant adjustments
Update your protocol anytime by asking the AI to regenerate specific sections based on your new requirements. Whether responding to an ethics committee's comments or changes in your study design, adapt your document in just a few clicks.
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Simple, transparent pricing that scales with your growth.
Recommended
Pro
Ideal for freelancers
Linked documents included
equivalent to
~ 300 pages written
Recommended
Plus
For strategic documents
Linked documents included
equivalent to
~ 600 pages written
Recommended
Business
Designed for teamwork
Linked documents included
equivalent to
~ 1 200 pages written
Entreprise
Plan tailored to fit your needs
Go from idea to complete protocol in a single session
Join the hundreds of researchers and physicians who have already transformed their writing process. With DocGenius, create robust, compliant clinical study protocols in a fraction of the usual time, while maintaining the scientific rigor your research deserves.
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