LMM supports healthcare suppliers through product classification, product registration, manufacturer or site registration, import permit preparation, shipment clearance, documentation review, and Med Grade Storage receiving coordination.
Classification review to determine the correct regulatory pathway for your product category in the UAE.
Authority-specific product registration support including documentation, submission, and follow-up.
Company and manufacturing site registration with UAE health authorities as required.
Initial import permit preparation before shipping, ensuring regulatory pre-approval.
Post-shipment clearance after AWB, BOL, or truck waybill is available, including inspection coordination.
Review and preparation of product artwork, labels, and regulatory documentation for UAE compliance.
Import permit and shipment clearance are handled as separate workflow stages. The applicable authority and document pathway depend on product category, shipment status, registration status, and regulatory requirement.
Applied for before shipping. This is the initial regulatory approval that authorizes the product to enter the UAE. Required documents include product registration, classification, and manufacturer documentation.
Applied for after shipping, once the Air Way Bill, Bill of Lading, or Truck Way Bill is available. Includes inspection coordination, customs documentation, duty and VAT handling, and release to Med Grade Storage.
Authority pathway may involve MOHAP, EDE, Dubai Municipality, Customs, FANR, or another applicable authority depending on product type and regulatory requirement.
Submit your product details and we will assess the classification, registration pathway, and clearance requirements.