Literature Review and CER Automation Platform
Transform your medical device compliance process with our fully automated platform for Literature Reviews and Clinical Evaluation Report (CER) generation. Save time and resources while ensuring exceptional accuracy and regulatory compliance.
Nvidia
Bloomberg
Sony
Unilever
Deutscen Bushhandels
Streamline Your Clinical Evaluation Process
AI-agent tools designed for medical device compliance
Effortlessly generate comprehensive Clinical Evaluation Reports.
Save time with data auto-populated from your analysis.
Ensure all regulatory requirements are met with integrated checklists.
Simplify the creation of Summary of SSCP documents.
Access and search across multiple medical databases to gather comprehensive and relevant data.
Receive AI-driven search query suggestions tailored to your specific medical device.
Ensure data integrity by eliminating duplicate entries.
Prioritize the most relevant studies with intelligent scoring.
Effortlessly generate Summary of Safety and Clinical Performance (SSCP) documents, reducing manual workload and ensuring EU MDR compliance.
Automatically verify that your SSCPs meet all regulatory standards, keeping you audit-ready and compliant with evolving requirements.
Create SSCPs in multiple languages to meet global regulatory demands, expanding your device’s reach and accessibility worldwide.
Keep your SSCPs current with real-time data integration, ensuring your documents reflect the most recent and accurate information.
Leverage cutting-edge AI for precise data extraction and content generation, enhancing efficiency in your compliance process.
Our AI systems are designed to prevent hallucinations, ensuring all generated content is accurate and based on verified data.
Combine AI efficiency with human expertise; maintain control and validate AI outputs for optimal accuracy and reliability.
Benefit from transparent AI decision-making with clear reasoning, supported by rigorous quality checks to guarantee excellence.
Why Choose SummarizeBot?
Average time savings in CER preparation
Accuracy in literature classification
Built for regulatory compliance
What makes Literature Review and CER Automation
platform unique?
End-to-End Automation
The platform fully automates the entire CER process, from literature search to final report, integrating every step.
Proprietary AI Technology
Our unique AI agents collaborate for comprehensive analysis and unmatched accuracy in evaluations.
Regulatory-First Approach
Built to meet EU MDR requirements,the platform updates regularly to align with changing regulations.
Industry-Leading Accuracy
Achieve 99.9% accuracy in literature classification, validated against over 10.000 manually reviewed papers.
Human-Centric AI
Our system combines AI efficiency with human expertise, keeping you in control throughout the process.
Free Customization and Training
Enjoy free customization and training with no onboarding fees, tailoring the platform to your specific project needs.
Collaboration Tools
Enhance teamwork with real-time editing, commenting, and task tracking within our knowledge management platform for writers.
Transparent Decision-Making
Our AI provides transparent processes, showing the basis of every recommendation and analysis for full accountability.
Top-Tier Security
Your data is protected with ISO 27001 certification, GDPR compliance, encryption, and regular audits for peace of mind.
How to start generating CERs?
Set Protocol
Configure your device-specific evaluation parameters
Upload Documentation
Upload a technical documentation and device files
Press Start
Initiate the automated evaluation process
Get Results
Receive your complete LTR, CER, or SSCP
Pricing
Features & Services |
Literature Review Platform |
Automated CER Generation |
Automated SSCP Generation |
|---|---|---|---|
| Starting Price (per project) |
|
|
|
| Core Features | |||
| Onboarding Costs | Free | Free | Free |
| Expert Validation | Human-in-the-Loop Support | PhD Level (from €10,000/CER) | PhD Level (from €1,000/SSCP) |
| Customization | Free & Easy | Advanced Templates | Basic Templates |
| AI Capabilities | |||
| Document Analysis | Full-Text Analysis at Every Stage | Input Validation & Categorization | Basic Analysis |
| AI Technology | Extractive AI Transparency | AI Agents & AI Judge | AI Translation |
| Language Support | Multiple Languages | Multiple Languages | Multiple Languages |
| Automation Features | |||
| Report Generation | Literature Review Reports | Full CER Generation | SSCP Generation |
| Quality Control | Automated Bias Detection | Expert Validation | Automated Checks |
| Data Processing | Duplicate Detection | Document Categorization | Translation Processing |
| Access & Support | |||
| Project Support | Unlimited | Unlimited | Unlimited |
| User Access | Unlimited | Unlimited | Unlimited |
| Export Options | Excel & Multiple Formats | Multiple Formats | Standard Formats |
Frequently asked questions
The Literature Review and CER Automation platform is a comprehensive platform that automates the clinical evaluation process for medical device companies, including literature reviews, report generation, and compliance management.
Our platform is built on a regulatory-first framework that automatically aligns with EU MDR requirements and other global standards.
We offer 24/7 technical support, dedicated customer success managers, and comprehensive training programs.
Book a demo to see how SummarizeBot can help you save time and ensure compliance.