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For sponsors and CROs

Clinical-trial device operations in Uzbekistan.

MEDEMBARK helps international teams plan and coordinate investigational-device movement, controlled handling, site supply, accountability, returns, and supporting records.

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Healthcare professionals observing a supervised clinical equipment training demonstration
Uzbekistan operations
01

Before shipment

  • Pre-shipment planning
  • Import documentation review
  • Customs coordination
  • Sponsor and courier communication
02

In-country handling

  • Controlled storage
  • Temperature records
  • Trial inventory
  • Site distribution
03

Accountability and close-out

  • Device accountability
  • Return coordination
  • Destruction coordination
  • Supporting documentation
04

Operational continuity

  • Local communication
  • Urgent operational support
  • Issue escalation
  • Agreed operational reporting

Process timeline

One operating record from scope to reconciliation.

The final workflow is adapted to the investigational device, study, sponsor procedures, sites, and applicable local requirements.

  1. 01

    Scope

    Confirm product, protocol, shipment, site, and documentation requirements.

  2. 02

    Plan

    Align import, courier, storage, monitoring, inventory, and delivery responsibilities.

  3. 03

    Receive

    Coordinate customs release and controlled receipt against the agreed shipment plan.

  4. 04

    Supply

    Manage inventory and documented delivery to authorised clinical sites.

  5. 05

    Reconcile

    Coordinate accountability, returns, destruction, and close-out documentation.

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Public inquiry forms must not contain patient names, health information, subject IDs, medical records, or sensitive trial data.