Clinical Teams, SMEs and CROs preparing Clinical/Performance Evaluation Reports
Problem
Manual literature review is slow, costly, and error-prone + A clear clinical strategy is business critical since it can decide if your medical device will actually enter & stay in the market.
Solution
CertHub takes care of the entire literature research and appraisal for your Clinical Evaluation Reports (CERs) accord. to Annex XIV MDR and Performance Evaluation Report (PER) accord. to Annex XIII IVD – freeing you from tedious work while you keep control over every decision.
More ressources for what matters...
0h
saved on manually reviewing papers
0%
faster review without sacrificing scientific integrity
0%
tracability of all papers used
Covering the four stages of Clinical Evaluation
Search Strategy Definition
Define your device category, intended use, classification, and key technical terms – we guide you through every step.
Literature Retrieval
We use AI agents to retrieve all relevant publications with full abstracts, metadata, traceable queries, and the underlying key questions.
Automated Abstract Screening
We use AI agents to read and classify according to clinically relevant criteria.
Full-Text Analysis
CertHub pulls structured data from your full-text PDFs and instantly drafts the clinical appraisal – summary tables, risk-benefit insights, and fully traceable references included.
We’ll walk you through...
Let's find out more about CertHub and see the Research Agent in action.
CertHub offers AI-fueled software solutions for Technical Documentation, QMS and Design Control - tailored to the MedTech industry.