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Clinical evidence, done right.
Faster.

CiteMed automates literature reviews, CERs, and post-market surveillance for medical device teams — cutting timelines, eliminating copy-paste errors, and keeping every submission audit ready.

BY THE NUMBERS

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Faster document creation
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Regulatory acceptance rate
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Audit package vs. 2 weeks
  • Trusted by medtech and pharma teams across startup to Fortune 500 scale. Every submission meets the highest scientific standards — with zero tolerance for data issues.

WHAT WE DO

  • Systematic literature reviews
    Full-cycle search to submission — PubMed, Embase, ClinicalTrials and more, with PRISMA-ready exports for MDR, IVDR, and FDA.
  • CER & regulatory document automation
    Smart templates auto-populated from master data, with a regulatory interpretation engine for multi-jurisdiction submissions.
  • Post-market surveillance (PMS)
    Safety signal detection, PSUR and SSCP generation, and competitor claim monitoring — all audit-ready.
  • CiteSource — unified evidence library
    One searchable repository for all clinical literature across teams. Eliminates duplicate purchases and keeps references traceable to every submission.

TAKE SOMETHING WITH YOU

Learning From Mistakes:

Common Pitfalls Of Clinical Evaluation Reports

AI in Medtech Clinical Evaluation:

A Practical Approach & Implementation Guide

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