NOÉ AI accelerator for your
literature reviews
Automate up to 70% of manual work. MDR/IVDR compliance. Traceability & auditability.
Supported by major players in health research and innovation
Benefit
A solution designed to meet the requirements of the healthcare sector, while simplifying daily work.
A smart web app
NOÉ accelerates systematic reviews through AI, automating search, screening, and synthesis while ensuring scientific rigor.
Measurable and concrete gains
more precise than other AI
time saved
poor studies dismissed
relevant studies detected
Features
NOÉ combines the power of AI with scientific rigor to automate the most time-consuming steps of your literature reviews.
AI Assistant
An AI toolbox designed to assist literature reviews, under human supervision.
Automated PRISMA
NOÉ automatically generates a clear and compliant representation of your systematic review process.
Keyword Highlighting
Keywords are highlighted in titles and abstracts to speed up document understanding.
Data Extraction & Summary
NOÉ extracts key information and creates clear, traceable summaries while preserving original sources.
Our vision
Discover how NOÉ is reinventing literature review to make it more reliable, faster, and collaborative.
Testimonials
Researchers and institutions use NOÉ to accelerate their systematic reviews and ensure the reliability of their analyses.
FAQ
Need more details? Here are the answers to the most frequently asked questions.
What is NOÉ?
NOÉ is a SaaS web platform designed to conduct systematic reviews of scientific literature and to prepare clinical evaluations — particularly in the field of medical devices. It automates time-consuming steps such as searching, screening, selection, data extraction, and synthesis in order to accelerate processing.
How does NOÉ differ from other literature review tools?
Unlike general-purpose tools, NOÉ has been designed to meet the regulatory requirements of the EU Medical Devices Regulation (MDR/IVDR), with a structured PRISMA methodology (search, screening, selection, extraction, reporting) compliant with PRISMA methodological standards (systematic review standards, traceability, auditability). It combines usability, explainable AI, workflows adapted to regulatory requirements, and the export of deliverables ready to be integrated into regulatory documentation.
How is AI used in NOÉ?
Artificial intelligence automates reference collection, initial screening, relevant article suggestions, deduplication, data extraction, and preliminary synthesis of results. The user retains a central role — final review, scientific validation, and interpretation remain human.
Does NOÉ replace the human expert?
No. NOÉ is designed to assist experts, not replace them. AI reduces repetitive workload and speeds up article identification, but critical analysis and scientific judgment remain the responsibility of the user.
Does NOÉ follow a standardized methodology (such as PRISMA / PICOS)?
Yes. NOÉ supports systematic review methods compliant with frameworks such as PRISMA and encourages the use of structured frameworks like PICOS, ensuring transparency, reproducibility, and methodological quality.
Is NOÉ compatible with MDR/IVDR requirements for medical devices?
Yes. NOÉ has been designed to support Clinical Evaluation Reports (CER/PER) compliant with EU MDR and IVDR, by structuring evidence collection and synthesis in line with regulatory expectations.
Do you offer a trial version?
Yes. A free 30-day trial is available, allowing users to test NOÉ and assess its suitability for their needs.