In a global market where timing is critical, discovering an FDA detention days too late can result in significant port fees and supply chain disruptions. LMG Compliance Monitor™ leverages advanced monitoring technology to conduct daily automated scans of official FDA databases on your behalf.
| Service Feature | Standard Industry Practice | LMG Compliance Monitor™ |
|---|---|---|
| Alert Speed | Discovering issues days later. | Verified Daily Detection Cycle. |
| Data Reliability | High "False Positive" rates. | Human-Verified by LMG Experts. |
| Service Cost | $500 - $2,000 annual fees. | FREE for LMG Clients. |
| Notification Type | Raw, unformatted data logs. | Factual Intelligence Briefs. |
LMG Compliance Monitor™ utilizes proprietary monitoring logic and a secure, high-availability cloud architecture to perform daily surveillance. By integrating automated data intelligence with rigorous human verification by our U.S.-based consultants, we provide a level of Import Intelligence that standard consulting firms cannot match.
LMG Compliance Monitor™ cross-references your specific firm registration details and product codes against the FDA's published refusal and detention databases.
No. This service is provided as a complimentary value-add for all active LMG FDA Registration and Consulting clients.
LMG Compliance Monitor™ performs a comprehensive scan of the FDA databases every 24 hours. This daily cycle ensures that our consultants can verify the data before you receive your factual notification.
Your firm is already being monitored. If you have questions about your surveillance status or need to update your contact information, please contact our FDA consulting team.
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