Compliant medical device data management
Automate classification of medical devices and extraction of clinical attributes while maintaining FDA compliance and regulatory standards.
Built for healthcare compliance
From medical devices to pharmaceutical products, maintain regulatory compliance at scale.
FDA Classification Compliance
Automatically classify medical devices according to FDA regulations with complete audit trails.
Clinical Attribute Extraction
Extract technical specifications, indications, and contraindications from clinical documentation.
Medical Supply Normalization
Standardize product data across multiple suppliers and manufacturers for consistent procurement.
Regulatory Documentation
Maintain compliant product data with structured attributes required for regulatory submissions.
Comprehensive medical device intelligence
Product Gale understands healthcare data—from FDA classifications to clinical specifications and compliance requirements. Automate what used to take weeks of manual work.
- FDA device classification (Class I, II, III)
- Clinical attribute extraction from IFUs and labels
- Medical supply catalog normalization
- UDI (Unique Device Identification) management
- Regulatory compliance tracking
- Multi-language medical terminology support
Medical distributor automates 50K+ device classifications
A healthcare distributor needed to classify and maintain compliance data for over 50,000 medical devices from multiple manufacturers. Product Gale automated FDA classification and clinical attribute extraction, reducing compliance review time by 90%.
Ready to streamline medical device data?
Start your free trial and discover how Product Gale can help you maintain compliant, structured medical device data at scale.