The AI Engine Behind Faster Evidence
Retrospective studies, comparative effectiveness, registry design, and pharmacovigilance — evidence beyond clinical trials.
Services
Everything Evidence, Under One Roof
Protocol Builder
Define your PICO framework, eligibility criteria, and search strategy with guided templates that follow PRISMA-P standards
Intelligent Search
Search 125M+ papers across PubMed, Embase, Cochrane, and 20+ additional databases simultaneously.
AI Screening
Automatically screen titles and abstracts against your inclusion criteria. Borderline cases flagged for human review.
Smart Data Extraction
AI extracts study characteristics, outcomes, and endpoints into structured forms — verified by human reviewers.
Quality Assessment
Built-in tools for Cochrane RoB 2, ROBINS-I, Newcastle-Ottawa, and GRADE certainty assessments.
Synthesis & Reporting
Generate narrative syntheses, forest plots, PRISMA flow diagrams, and publication-ready reports automatically.
Deliverables
Manual Process vs. AnswerThis
Metric
Manual Process
AnswerThis Platform
Timeline (full SLR)
6–18 months
2–6 weeks
Databases searched
3–5 manually
20+ simultaneously
Screening throughput
~100 papers/day/person
~5,000 papers/hour (AI)
Data extraction accuracy
Varies by reviewer
95%+ AI + human verified
PRISMA compliance
Manual checklist
Built-in automated checks
Cost per review
$50K–$200K+
Significantly lower
Deliverables
Built for sciences
Clinical Evaluation Reports
Structured data capture
Post-Market Clinical Follow-Up
PMCF literature reviews for ongoing regulatory compliance.
Equivalence Assessments
Structured comparator analyses for 510(k) and CE marking submissions.
Health Technology Assessments
Evidence packages tailored for MedTech-specific HTA requirements.
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AI-powered evidence generation for life sciences. Structured literature reviews, HEOR, market access, and reimbursement strategy — delivered end-to-end.
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