About us
English
AI Research Assistant for Healthcare
Accelerate clinical research workflows with an AI research assistant for healthcare that summarizes evidence, drafts protocols, and organizes insights.
AI powered (Demo)
1
Add a file
Drop in anything you'd like to use.
OR TRY WITH A SAMPLE
2
Pick a prompt
Add a file first — then any prompt runs against it.
By using the product, you agree to our Terms of Service and have read our Privacy Policy.
Trusted by Millions Worldwide
4.4
2,100+ reviews on G2
4.4
8,200+ reviews on Capterra
4.4
73,000+ reviews on App Store
248M
Registered Users
5B
Notes Created
2M
Notes Created Daily
Frequently Asked Questions
An AI research assistant is a tool that helps healthcare professionals process and organize clinical and research materials. It can summarize documents, extract key findings, draft protocols, and suggest next steps, making Evernote workflows faster and more focused for clinical research teams.
For clinical research, the assistant can synthesize literature, generate study outlines, standardize data extraction fields, and create operational checklists. It helps teams turn scattered notes and meeting minutes into structured plans, saving time when preparing protocols, manuscripts, or grant proposals.
Yes. The assistant can produce concise summaries, bullet-point key takeaways, or multi-level abstracts from long notes. You can ask for a three-bullet brief, a one-paragraph executive summary, or a detailed section-by-section condensation tailored to your audience.
It can draft study protocol templates and populate common sections (objectives, design, outcomes, sample size logic) from your notes. Teams should review and adapt these drafts for local context and regulatory requirements before submission to IRB or sponsors.
Yes. The assistant can rewrite technical content into patient-facing language, create consent script drafts, and produce one-page handouts in clear, accessible terms. You can specify reading-level targets and languages to tailor materials to your patient population.
It can propose data dictionaries and form templates based on study aims and outcomes described in your notes. These templates can include field names, coding conventions, and suggested validation rules that you can export and adapt for your REDCap or EHR integration.
Yes, you can upload PDFs and slide decks into Evernote; the assistant will extract text and images where supported and use them to build summaries, extract citations, and generate action items. For scanned documents, OCR quality affects extraction fidelity.
Yes. Provide the relevant documents or notes and ask for a side-by-side comparison. The assistant can summarize comparative effectiveness, highlight differences in populations, outcomes, and implementation needs, and list evidence quality caveats.
It can help draft sections of grant proposals-background, aims, methods, and workplans-based on your notes and prior drafts. Use its output as a starting point and verify figures, budgets, and compliance language before submission.
The assistant can outline slide content and suggest bullet points, visuals, and speaker notes from your notes. You can then export the outline into your preferred slide software and refine design and data visualizations for presentations.
Yes. The assistant can scan documents for common limitations-small samples, short follow-up, lack of blinding, or poor generalizability-and summarize these for methods and discussion sections, helping prepare balanced interpretations.
It can parse your notes to list action items, suggested owners, and deadlines. If your notes include names and due dates, the assistant will surface them as a task list you can copy into project trackers or Evernote reminders.
The assistant extracts citation metadata when available and can format references into common styles. It is best to cross-check extracted DOIs and page numbers against your reference manager before final submission.
The assistant depends on the quality and completeness of your source notes. It generates drafts and suggestions that require domain expert review, especially for clinical decisions, regulatory documents, and final manuscripts. Use outputs as a starting point and validate critical details manually.