IMDRF Coding System - Complaint Classification Tool
IMDRF Complaint Coding System is an advanced AI-powered software designed to assist Post-Market Surveillance Teams in accurately coding complaints using the internationally recognized IMDRF A to G Codes. The software leverages state-of-the-art Natural Language Processing (NLP) to analyze complaint descriptions, investigation summaries, and patient impact data, providing highly relevant IMDRF codes for regulatory reporting.
This tool is particularly useful for:
- Medical Device Manufacturers ensuring compliance with US FDA MDR (Medical Device Reporting) and other global regulatory agencies.
- Regulatory Affairs Professionals streamlining post-market surveillance and adverse event reporting.
- Quality & Compliance Teams improving complaint coding accuracy and reducing manual effort.
Key Features:
✔ AI-powered semantic search for IMDRF coding recommendations.
✔ Intuitive two-panel UI for easy complaint entry and code selection.
✔ Supports A to G Codes based on IMDRF regulatory standards.
✔ Helps in compliance with FDA & global regulatory reporting requirements.
✔ Instant confidence scores for recommended codes.
💰 Price: $99
📥 Instant Digital Download
✔ Tool Screenshot:
A powerful AI-driven IMDRF Complaint Coding System designed for Post-Market Surveillance Teams and Regulatory Professionals. This software helps medical device companies accurately classify and report complaints using IMDRF A-G Codes, ensuring compliance with US FDA MDR reporting and other regulatory requirements.