Stop Losing Months to Manual Literature Reviews

Stop Losing Months to Manual Literature Reviews

Stop Losing Months to Manual Literature Reviews

AnswerThis gives pharma, biotech, and medical device teams a single platform to find evidence, run systematic reviews, and produce submission-ready documentation

AnswerThis gives pharma, biotech, and medical device teams a single platform to find evidence, run systematic reviews, and produce submission-ready documentation

Trusted by over 200,000+ researchers

  • Christopher newport university
  • SAIT
  • MIT
  • Penn
  • Standford university
  • University of oxford
  • NASA
  • Christopher newport university
  • McKmsey & Company

Trusted by 200,+ institutions and individuals

  • Christopher newport university
  • SAIT
  • MIT
  • Penn
  • Standford university
  • University of oxford
  • NASA
  • Christopher newport university
  • McKmsey & Company

Trusted by 200,000+ institutions and individuals

  • Christopher newport university
  • SAIT
  • MIT
  • Penn
  • Standford university
  • University of oxford
  • NASA
  • Christopher newport university
  • McKmsey & Company

Enterprise-Grade Infrastructure, Built In From Day One

Every plan comes with the security, privacy, and scale your organization demands — no add-ons, no upgrades required.

Enterprise-Grade Infrastructure, Built In From Day One

Every plan comes with the security, privacy, and scale your organization demands — no add-ons, no upgrades required.

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

Unlike consumer AI tools, nothing your team uploads, searches, or writes is ever used to improve our models. Your IP stays yours.

Access Over 250 Million+ Abstracts

Search across PubMed, Embase, Scopus, and hundreds of databases from a single interface. No gaps, no switching between platforms.

Works With Your Library Subscription

Connects directly 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 integration so your IT team can deploy across departments without managing individual accounts

Everything Your Resarch Team Needs To Move Faster

Purpose-built tools for every stage of the pharma research lifecycle — from evidence discovery to regulatory deliverable.

Everything Your Resarch Team Needs To Move Faster

Purpose-built tools for every stage of the pharma research lifecycle — from evidence discovery to regulatory deliverable.

Find evidence for claims

Search 300M+ papers with precision filters for population, intervention, comparator, and outcome. Surface the exact evidence your regulatory team needs to support label claims, safety profiles, and therapeutic positioning.

Find evidence for claims

Search 300M+ papers with precision filters for population, intervention, comparator, and outcome. Surface the exact evidence your regulatory team needs to support label claims, safety profiles, and therapeutic positioning.

Systematic Literature Reviews

Run PRISMA-compliant systematic reviews end-to-end — protocol, search, screening, extraction, quality assessment, and narrative synthesis — in one platform. Every step is logged with full audit trails for regulatory inspection.

Systematic Literature Reviews

Run PRISMA-compliant systematic reviews end-to-end — protocol, search, screening, extraction, quality assessment, and narrative synthesis — in one platform. Every step is logged with full audit trails for regulatory inspection.

Data Analysis & Extraction

Extract structured data points from included studies into standardized evidence tables. Custom columns for your protocol-specific variables. Export directly into formats ready for FDA, EMA, or PMDA submissions.

Data Analysis & Extraction

Extract structured data points from included studies into standardized evidence tables. Custom columns for your protocol-specific variables. Export directly into formats ready for FDA, EMA, or PMDA submissions.

Medical Coding & Classification

Organize extracted findings by MeSH terms, ATC codes, and ICD classifications. Standardize terminology across your evidence base so nothing gets lost in translation between teams.

Medical Coding & Classification

Organize extracted findings by MeSH terms, ATC codes, and ICD classifications. Standardize terminology across your evidence base so nothing gets lost in translation between teams.

Value analysis

Build evidence-backed value dossiers and HTA-ready assessments.

Value analysis

Build evidence-backed value dossiers and HTA-ready assessments.

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.

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.

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

Results Your Team Will Actually Feel

Less time screening, fewer missed deadlines, and research outputs that hold up under regulatory scrutiny.

Results Your Team Will Actually Feel

Less time screening, fewer missed deadlines, and research outputs that hold up under regulatory scrutiny.

Results Your Team Will Actually Feel

Less time screening, fewer missed deadlines, and research 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/exclusion decision, every extraction, every quality assessment is timestamped and attributed. When regulators ask for your methodology, you hand them a complete log — not a reconstructed narrative.

Reduce CRO Dependency

Stop outsourcing every review at $100K+ per project. Your internal team can produce the same quality of output with AnswerThis, keeping institutional knowledge in-house and timelines under your control.

Cross-Therapeutic Area Consistency

Whether your team is working on oncology, rare disease, or cardiovascular, the same standardized workflow applies. No more inconsistent methods across therapeutic areas.

See What Your Team Saves

The average systematic literature review takes 6–18 months and costs $150,000+ in researcher time. AnswerThis cuts that by up to 90%.

See What Your Team Saves

The average systematic literature review takes 6–18 months and costs $150,000+ in researcher time. AnswerThis cuts that by up to 90%.

Reviews per year4
120
Avg. team size per review5
115

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

Frequently asked question

Your Questions Answered.

What is AnswerThis?

AnswerThis is an all-in-one AI research assistant that supports your entire workflow, from finding research gaps and collecting papers to summarizing, analyzing, and drafting citation-backed content for your research paper, dissertation, or thesis.

How can AnswerThis support my clinical research workflow?

How many research papers can I access?

Can I organize my research?

Does AnswerThis help with literature reviews?

Can AnswerThis format citations automatically?

Is AnswerThis suitable for all levels of research?

How does AnswerThis draft research content?

Is my data secure?

Your Questions Answered.

What is AnswerThis?

AnswerThis is an all-in-one AI research assistant that supports your entire workflow, from finding research gaps and collecting papers to summarizing, analyzing, and drafting citation-backed content for your research paper, dissertation, or thesis.

How can AnswerThis support my clinical research workflow?

How many research papers can I access?

Can I organize my research?

Does AnswerThis help with literature reviews?

Can AnswerThis format citations automatically?

Is AnswerThis suitable for all levels of research?

How does AnswerThis draft research content?

Is my data secure?

Your Questions Answered.

What is AnswerThis?

AnswerThis is an all-in-one AI research assistant that supports your entire workflow, from finding research gaps and collecting papers to summarizing, analyzing, and drafting citation-backed content for your research paper, dissertation, or thesis.

How can AnswerThis support my clinical research workflow?

How many research papers can I access?

Can I organize my research?

Does AnswerThis help with literature reviews?

Can AnswerThis format citations automatically?

Is AnswerThis suitable for all levels of research?

How does AnswerThis draft research content?

Is my data secure?