Powered by machine learning models on 6 million complaints, it will automatically categorizes complaints according to MDCG-recommended
IMDRF Adverse Event Terminology and FDA Event Type.
Discover how SmartComplaints can transform your complaint categorization process. Instant categorization of complaints according to IMDRF Annex A and E Codes and FDA Type.
Try SmartComplaintsTMRegulatory Compliance
Immediate categorization
Efficient Audits
Proper categorization streamlines root cause analysis, improving efficiency and effectiveness of corrective actions.
Ensure Medical Device Coordination Group (MDCG) & IMDRF standards.
Facilitates standardized reporting across different markets, minimizing regulatory delays.
Accurate use of IMDRF Annex codes improves traceability and simplifies the audit process.