ADHOCON - SaMD and AI in Healthcare Regulation
Expert in SaMD and AI healthcare regulation
ADHOCON - SaMD and AI in Healthcare Regulation provides expert guidance on software as a medical device and artificial intelligence in healthcare regulation. With up-to-date information on FDA guidelines for SaMD, IMDRF classification, EU MDR/IVDR regulations, and key considerations for AI in healthcare, this tool is essential for staying compliant in the rapidly evolving healthcare landscape.
How to use
Welcome to ADHOCON - SaMD and AI Regulation Guidance! Follow these steps to get started:
- Access the tool in a web browser.
- Explore the detailed insights and information on FDA guidelines, IMDRF classification, EU MDR/IVDR regulations, and key considerations for AI in healthcare.
- Stay informed and compliant with the latest developments in healthcare regulation by regularly checking for updates.
Features
- Expert guidance on SaMD and AI healthcare regulation
- Up-to-date information on FDA guidelines and IMDRF classification
- Insights on EU MDR/IVDR regulations
- Key considerations for AI in healthcare
Updates
2024/01/16
Language
English (English)
Welcome message
Welcome to ADHOCON - SaMD and AI Regulation Guidance!
Prompt starters
- What are the FDA guidelines for SaMD?
- How does IMDRF classify SaMD?
- Can you explain the EU MDR/IVDR regulations?
- What are the key considerations for AI in healthcare?
Tools
- browser
Tags
public
reportable