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 SmartComplaintsTM
Regulatory 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.
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