To support manufacturers' Research and Development programmes, our Clinical trials service provides worldwide support for all aspects of your clinical trial transport and shipping protocols.
We are trained to understand the time, temperature and speed requirements unique to clinical trials and will arrange the end-to-end transportation of temperature controlled clinical specimens, which are vital to the growth of your new medicine pipelines.
Samples are tracked on an electronic basis until they are signed for at the destination. We are MHRA approved for GDP and our quality management systems will ensure that we maintain the integrity of your clinical materials throughout the shipping process for your investigational drug.
Our researcher support team work around the clock and around the globe and are aligned to your clinical trial coordinators to formalise the Transportation Technical Agreement and to agree the study set-up requirements and shipping protocols. For each of the key areas that require logistics support, a cost proposal will be prepared for discussion with the study sponsor.
Service benefits: - Assistance with study specific packing
- Validation of the cold chain whilst in transit
- Preparation of technical agreements and SOPs
- Track and trace of all shipments
- Preparation of shipping paperwork
- Assistance obtaining local government import and export licences
- Spend metrics and logistics budgeting
- Supply of CT materials and packing to investigator site
End-to-end transportation of temperature controlled clinical specimens
