Our dedicated clinical trails staff are trained to understand the essential time, temperature and speed requirements that are unique to clinical trials. We 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 electronically until they are signed for at their 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.
Our support team works around the clock, and around the globe, and liaises directly with your clinical trial coordinators to formalise the Transportation Technical Agreement and to agree the study set-up requirements and shipping protocols.
For each key area of the trial that requires logistics support, a cost proposal will be prepared for discussion with the study sponsor.
End-to-end transportation of temperature controlled clinical specimens
