Pharmaceutical >> Clinical Trial Support >> Clinical Trial Materials Management

Clinical Trial Materials Management

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Pharmaceutical services for clinical trials

A storage area of 850 m2 and a technical platform recognized for the assurance of a quality clinical trial logistics service.

To ensure a high quality service, Eurofins Pharma Quality Control dedicates to its clinical trial logistics activity a large infrastructure fully equipped for the care of all your experimental drugs. In addition to a wide range of storage conditions at controlled temperature, Eurofins Pharma Control provides you all pharmaceutical manufacturing operations, distribution and logistics of your treatment units, your medical devices and documents for clinical trials.

Combining responsiveness, reliability and traceability, and a vast experience in the cold chain, Eurofins Pharma Control handles logistics of your pharmaceuticals, nutraceuticals and cosmetics.

Clinical GMP status activity

Eurofins Pharma Quality  Control provides you the following manufacturing operations:

  • Importation of goods for clinical trials from and outside the European Community
  • Technical batch release
  • Secondary packaging of drugs for patients. We create these packages in order to best meet the specific requirements of the study
  • Randomization and labeling of boxes
  • Stability study of clinical batches (storage and analysis) and extension of expiry date

Clinical GDP status activity

Eurofins Pharma Control supports all operations for the distribution of your products:

  • Dispatch to centers (hospitals and medical offices) via specialized carriers
  • Replenishment of supplies
  • Return, reconciliation and destruction of remaining products
  • Establishment of monitoring temperature in investigator centers with providing of necessary software for metrological control
  • Qualification of refrigerators and other forums in the investigator centers
  • Insulated transport packages validated summer, winter, mid season
  • Storage in controlled conditions (-80°C, -20°C, +4°C, +20°C)

Logistics of biological samples

  • Constitution and sending on-site of sampling kits
  • Transport of samples in compliance with regulations (ADR, IATA)
  • Storage in controlled conditions (-80°C et -20°C)
  • Monitoring of serum bank

Strong logistical services:

  • Specific quality system
  • Large qualified facilities in controlled conditions
  • Strong reactivity (shipment 24/72h in Europe)
  • Batch tracking and storage and shipment temperature monitoring
  • Important knowledge in cold chain and temperature traceability
  • Validated packaging system
  • Large experience in monitoring clinical trials