Clinical Distribution

Clinical Distribution Cold Chain Management Depot Network Return & Destruction

Our comprehensive clinical batch distribution package includes:

  • Carrier qualification and management
  • Import and export, including customs clearance
  • GMP/GDP storage
  • Distribution and returns management
  • Quality assurance support

We are authorized to transport:

  • IMPs, IVPs
  • Controlled drugs
  • Dangerous goods according to IATA classification

We are also used to handling:

  • Ancillary supplies
  • Documentation (case report forms)
  • All quantities and parcel sizes
  • Ambiant and controlled temperature shipments (+15°C/+25°C, +2°C/+8°C, -20°C, -80°C)

We are able to advise clients on the best shipping strategies depending on the location of the investigational sites.
Our detailed knowledge of our audited carriers enables us to suggest a supply chain solution and a suitable carrier, taking into consideration their capacity and expertise in the destination countries.

We select carriers, sign contracts and QA agreements with them, and continually monitor their performance. We choose the best carrier for each shipment depending on: the type of product to be transported, the delivery deadline, the destinations, and the required transport conditions.

Our dedicated distribution team is IATA trained (dangerous goods).

To ensure full traceability, we use Gexpec software (a commercial software solution dedicated to the distribution of clinical trial products and materials) for:

  • Deliveries
  • Receipts
  • Storage
  • Shipments
  • Pickup and receipt of returns

Clients have personal secure web access to their logistics data via a specific site, which is updated daily.

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