6+ months
Study Protocol Development
Manual literature reviews, database queries, and protocol writing consume valuable research time.
Build PICO-based study protocols, manage evidence from PubMed and clinical trial registries, run PRISMA-compliant reviews, and export regulatory-ready packages.
Free to use. No credit card required.
Traditional approaches to vaccine RWE studies are slow, expensive, and error-prone.
Manual literature reviews, database queries, and protocol writing consume valuable research time.
Screening hundreds of papers manually is slow and prone to human error.
Senior epidemiologist time, database access, and regulatory compliance add up fast.
Purpose-built for vaccine effectiveness and safety studies
Create PICO-based study protocols with structured fields for population, intervention, comparator, and outcomes.
Import from PubMed, ClinicalTrials.gov, and CrossRef. Organize with tags, filters, and full-text search.
FDA IND packages, eCTD Module 5, CDISC/SDTM templates, CONSORT/STROBE checklists — one click.
Generate PICO frameworks, synthesize evidence, and get AI-powered recommendations for your study design.
Real-time co-editing with presence indicators, comments with @mentions, and version history tracking.
PRISMA-compliant screening pipeline, risk-of-bias assessment, meta-analysis with forest plots.
A streamlined workflow that replaces months of manual work
Enter your research question using PICO framework fields.
Search PubMed and clinical trial registries from one interface.
Screen evidence, assess risk of bias, and co-edit with your team.
Generate FDA IND, eCTD, or SDTM packages ready for submission.
Create your first protocol in minutes. Import evidence from PubMed, screen studies, and export regulatory-ready reports.
Free to use. No credit card required.