Meddev
Faster Evidence Pipelines. Every Claim Verifiable.
Every industry has unique evidence demands. See how AnswerThis solves yours.
Trusted by over 200,000+ researchers
02
75% Less Time Finding Relevant Literature
Private by default. Audit-ready by design.
The non negotiables your IT and compliance teams check first.
Your data stays yours
We do not train on your data. Model providers hold zero retention.
Audit-ready on every decision
Every screening call and extraction logged with source passages.
Verifiable sources, every claim
Click a citation, see the exact sentence in the paper.
What medical devices teams build
Real workflows, running today.
CER Reviews
MEDDEV 2.7/1 Rev.4 clinical evidence sections
PMCF Monitoring
Ongoing surveillance per MDR Article 61(11)
Equivalence
Predicate device comparison analysis
510(k) Support
Substantial equivalence for FDA
SOTA Benchmarking
Performance and safety thresholds
Portfolio Scale
Workflows across your full device range
Why Meddev Teams Are Using AnswerThis Over Outsourcing
One evidence base, every team.
Regulatory, medical, HEOR, and commercial pulling from the same library.
Submission-grade defensibility.
Every decision logged. Every claim source-linked. Audit-ready by default.
The budget stays for work that actually needs specialists.
External hands for external work. In house capacity for everything else.
