The AI kit for Medical Writers

Verifies a claim, rates the source, and flags bias. Example: checking that a cited 12% risk reduction matches the trial paper.

Polishes abstracts, sections, references, and figures for submission. Example: turning rough reviewer notes into a clean revised discussion.

Checks quotes, statistics, dates, and originality before publication. Example: confirming a quoted mortality figure against the original study.

Drafts and validates case reports, diagnostic reports, and CSRs against CARE, ICH-E3, and HIPAA. Example: de-identifying a patient case report.

Like "Summarize Research Findings"

Like "Draft CSR Methods Sections"

Like "Outline Regulatory Submission Modules"

Like "Write a Patient-Friendly Education Leaflet"

Patients only receive the current approved version in every language.

An up-to-date evidence map with every new study screened.

Every working file references the current approved protocol version, with procedure changes decided by the investigator.

A reviewer response where every claim points to a real change.

Let your AI search medical research papers on PubMed and give you plain-English summaries.

Lets your AI search Google Scholar and pull ready-made citations for papers you find.

Let your AI edit real Word documents: text, tables, tracked changes, citations and more.

Let your AI edit Word, PowerPoint and Excel files, with changes you can review before saving.

Sourcely is an AI-driven tool that streamlines academic research by quickly sourcing relevant papers, summarizing content, and exporting citations from a databa

Grammarly enhances your writing with AI-driven checks on grammar, spelling, punctuation, and style, usable across over 500,000 platforms like Word and Gmail. It

Paperguide uses AI to simplify research by providing quick summaries, enabling efficient literature reviews, organizing references, and improving academic writi

GPT-4 Turbo offers advanced AI language capabilities with knowledge up to April 2023 and a 128k token context window, enabling it to process and generate detail

Keeps sources, drafts, and approvals in one owned workspace so you stop switching tools mid-manuscript.

Cuts rework between draft and approved copy while keeping your sources and voice intact.

Links every draft to its sources and keeps brand voice attached, practical for patient materials.

Checks both reference identity and the associated factual claim.

Writes clinical reports with regulatory compliance and validation tools.

Drafts full-paragraph scientific manuscripts using IMRAD structure with verified citations and figures.

Conducts systematic literature reviews across scientific databases and produces formatted documents.

Generates publication-ready clinical decision support documents for pharmaceutical research and evidence synthesis.