BIOCARD operates GDP-aligned processes designed to support client quality requirements: documented shipment plans, controlled packaging and conditioning, monitored transport, and per-shipment temperature records retained for review.
Packaging, PCM conditioning, monitoring and contingency actions are defined before movement in a shipment-specific Temperature Condition Plan.
Monitored shipments close with a temperature record and delivery report; records are retained and available for client review and investigations.
Packing, conditioning and handover steps follow written procedures, with training for the people who execute them.
We state what is included and what is not. Regulated materials move only with correct classification, documentation and carrier acceptance.
Legal entity, licence scope and certificate details are published here as they are verified and issued; current documentation is available to clients on request. UAE regulatory requirements for the transport, storage and distribution of medical products (including the 2023 ministerial requirements and the updated 2025 federal framework) inform how shipment plans are designed.
We answer questionnaires with what we actually do — if an item is outside our current scope, we say so and propose how it can be covered.
The deliverable your auditors actually want: the record.
Tell us about the shipment. A BIOCARD specialist will review the route, temperature requirement and shipment details before responding.
