Your Data Stays Private
Your research data is never used to train our models. Full data isolation, encrypted at rest and in transit.
Doesn't Train on Your Data
Nothing your team uploads, searches, or writes is used to improve our models. Your IP stays yours.
Access Over 250 Million+ Abstracts
PubMed, Embase, Scopus, ClinicalTrials.gov, and hundreds more from a single interface. No gaps, no platform-switching.
Works with your library subscription
Connects to your institution's existing journal subscriptions so your team gets full-text access without extra licensing.
Built for Enterprise Workflows
Role-based access, shared workspaces, project-level permissions, and audit trails designed for regulated teams.
SSO, SAML & Institutional Auth
Single sign-on so your IT team can deploy across departments without managing individual accounts.
Built for regulated industries
When your work feeds into FDA submissions, EMA dossiers, and HTA evaluations, your tools need to meet the same standard your reviewers do.
Metric
Premium
Enterprise
Searches
Unlimited
Unlimited
Citations
Line-by-line
Line-by-line
AI Writer
Unlimited
Unlimited
Library
Full
Full + shared
Data Extraction
Export
Export + custom columns
Risk of Bias (RoB 2)
—
Full assessment
Evidence Grading (GRADE)
—
Full framework
Research Alerts
—
Automated monitoring
Integrations
Zotero, Mendeley
Zotero, Mendeley, SSO, SAML, LIMS
Team Access
-
Organization-wide
Audit Trails
-
Full logging
Dedicated Support
-
Onboarding + success manager
Compliance
-
SOC 2, HIPAA-aligned
Same Quality, Less Time, Less Cost
Less time screening, fewer missed deadlines, and outputs that hold up under regulatory scrutiny.
10x Faster Reviews
What used to take 6–18 months now takes days to weeks. Automated screening, deduplication, and extraction eliminate the manual bottleneck without sacrificing thoroughness.
Audit-ready from day one
Every inclusion decision, every extraction, every quality assessment is timestamped and attributed. When regulators ask, you can export a complete log.
Reduce agency dependency
Your internal team produces the same quality output, keeping institutional knowledge in-house and timelines under your control.
Cross-Therapeutic Area Consistency
Oncology, rare disease, cardiovascular, the same standardized workflow applies. No more inconsistent methods across therapeutic areas.
Estimated annual savings with AnswerThis
Hours saved
22Kh
540 weeks of work eliminated
Cost saved
$1.8M
At $85/hr avg. researcher rate
Time to results
125 mo
Faster delivery per review cycle
