Evidence Research Built for Your Industry
Every industry has unique evidence demands. See how AnswerThis solves yours.
Trusted by over 200,000+ researchers
250M+
PAPERS INDEXED
80%
FASTER DELIVERY
95%+
EXTRACTION ACCURACY
PRISMA
COMPLIANT
Evidence Research Built for Your Industry
Every industry has unique evidence demands. See how AnswerThis solves yours.
Trusted by over 200,000+ researchers
250M+
PAPERS INDEXED
80%
FASTER DELIVERY
95%+
EXTRACTION ACCURACY
PRISMA
COMPLIANT
Trusted by over 200,000+ researchers
Trusted by 200,+ institutions and individuals
Trusted by 200,000+ institutions and individuals
Services
Everything Evidence, Under One Roof
Whether you need the complete output delivered or the software to do it yourself, AnswerThis is built for how evidence generation actually works.
125M+ papers searched
Our AI searches PubMed, Embase, Cochrane, Web of Science, and 20+ databases simultaneously — ensuring comprehensive coverage no manual search can match.
95%+ Extraction Accuracy
AI-powered data extraction validated by dual-reviewer verification. Every data point is traceable to its source with full provenance tracking.
80% Faster Than Manual
What traditionally takes 6–18 months is delivered in weeks. We compress timelines without sacrificing the rigour HTA bodies expect.
Pharmaceutical
Submission-ready SLRs in weeks, not months
AI screens 10,000+ abstracts, extracts data, and generates audit-ready evidence packages for FDA, EMA, and HTA submissions.
NDA/BLA submission evidence
Label expansion support
Post-market safety monitoring
HEOR value dossiers
FDA
EMA
PMDA
PRISMA
GRADE
Cochrane
Pharmaceutical
Submission-ready SLRs in weeks, not months
AI screens 10,000+ abstracts, extracts data, and generates audit-ready evidence packages for FDA, EMA, and HTA submissions.
NDA/BLA submission evidence
Label expansion support
Post-market safety monitoring
HEOR value dossiers
FDA
EMA
PMDA
PRISMA
GRADE
Cochrane
Pharmaceutical
Submission-ready SLRs in weeks, not months
AI screens 10,000+ abstracts, extracts data, and generates audit-ready evidence packages for FDA, EMA, and HTA submissions.
NDA/BLA submission evidence
Label expansion support
Post-market safety monitoring
HEOR value dossiers
FDA
EMA
PMDA
PRISMA
GRADE
Cochrane
Biotechnology
Full SLR capability without a full department
One researcher, one platform. Publication-quality reviews in days. No CRO dependency, no six-month timelines.
IND-enabling literature reviews
Competitive landscape mapping
Target validation synthesis
Investor-ready evidence packages
FDA IND
EMA PRIME
Orphan Drug
Breakthrough
Biotechnology
Full SLR capability without a full department
One researcher, one platform. Publication-quality reviews in days. No CRO dependency, no six-month timelines.
IND-enabling literature reviews
Competitive landscape mapping
Target validation synthesis
Investor-ready evidence packages
FDA IND
EMA PRIME
Orphan Drug
Breakthrough
Biotechnology
Full SLR capability without a full department
One researcher, one platform. Publication-quality reviews in days. No CRO dependency, no six-month timelines.
IND-enabling literature reviews
Competitive landscape mapping
Target validation synthesis
Investor-ready evidence packages
FDA IND
EMA PRIME
Orphan Drug
Breakthrough
Medical Devices
CER evidence at portfolio scale
Automate annual CER updates, equivalence searches, and PMCF monitoring across every device in your portfolio.
CER literature reviews (MEDDEV 2.7/1)
PMCF literature monitoring
Equivalence evidence searches
510(k) literature support
EU MDR
IVDR
510(k)
MEDDEV 2.7/1
PMCF
Medical Devices
CER evidence at portfolio scale
Automate annual CER updates, equivalence searches, and PMCF monitoring across every device in your portfolio.
CER literature reviews (MEDDEV 2.7/1)
PMCF literature monitoring
Equivalence evidence searches
510(k) literature support
EU MDR
IVDR
510(k)
MEDDEV 2.7/1
PMCF
Medical Devices
CER evidence at portfolio scale
Automate annual CER updates, equivalence searches, and PMCF monitoring across every device in your portfolio.
CER literature reviews (MEDDEV 2.7/1)
PMCF literature monitoring
Equivalence evidence searches
510(k) literature support
EU MDR
IVDR
510(k)
MEDDEV 2.7/1
PMCF
Contract Research Organizations
3× more engagements. Same team. Better margins.
AI handles screening and extraction volume. Your writers focus on analysis and narrative. Quality stays consistent.
Client SLRs & targeted reviews
HTA submission evidence
Rapid evidence assessments
NMA data extraction support
PRISMA
GRADE
Cochrane RoB 2
ROBINS-I
NOS
Medical Devices
3× more engagements. Same team. Better margins.
AI handles screening and extraction volume. Your writers focus on analysis and narrative. Quality stays consistent.
Client SLRs & targeted reviews
HTA submission evidence
Rapid evidence assessments
NMA data extraction support
PRISMA
GRADE
Cochrane RoB 2
ROBINS-I
NOS
Contract Research Organizations
3× more engagements. Same team. Better margins.
AI handles screening and extraction volume. Your writers focus on analysis and narrative. Quality stays consistent.
Client SLRs & targeted reviews
HTA submission evidence
Rapid evidence assessments
NMA data extraction support
PRISMA
GRADE
Cochrane RoB 2
ROBINS-I
NOS
HTA & Payer Organizations
One search. Every HTA body format.
Dossier evidence aligned to NICE, G-BA, HAS, and CADTH. Fully reproducible methodology. Zero gaps at submission.
NICE STA evidence packages
G-BA AMNOG Module 4
NMA literature support
Economic model inputs
NICE
G-BA / IQWiG
HAS
CADTH
PBAC
TLV
HTA & Payer Organizations
One search. Every HTA body format.
Dossier evidence aligned to NICE, G-BA, HAS, and CADTH. Fully reproducible methodology. Zero gaps at submission.
NICE STA evidence packages
G-BA AMNOG Module 4
NMA literature support
Economic model inputs
NICE
G-BA / IQWiG
HAS
CADTH
PBAC
TLV
HTA & Payer Organizations
One search. Every HTA body format.
Dossier evidence aligned to NICE, G-BA, HAS, and CADTH. Fully reproducible methodology. Zero gaps at submission.
NICE STA evidence packages
G-BA AMNOG Module 4
NMA literature support
Economic model inputs
NICE
G-BA / IQWiG
HAS
CADTH
PBAC
TLV
Ready to get started
Tell us about your project and we'll show you how we can help.
Ready to get started
Tell us about your project and we'll show you how we can help.
Ready to get started
Tell us about your project and we'll show you how we can help.
AI-powered evidence generation for life sciences. Structured literature reviews, HEOR, market access, and reimbursement strategy — delivered end-to-end.
© 2026 AnswerThis. All rights reserved.
AI-powered evidence generation for life sciences. Structured literature reviews, HEOR, market access, and reimbursement strategy — delivered end-to-end.
© 2026 AnswerThis. All rights reserved.