clinical trial services

Since 2002, Cryosite has expanded its range of services to include the provision of clinical supply management services to the pharmaceutical and clinical research organisations. Over the past 12 months, operations have increased steadily and already Cryosite have established a strong client profile.

The pharmaceutical industry now recognises the value of outsourcing. Outsourcing the management of clinical trial supplies and samples plays a particularly important role in clinical development and allows CRO’s, doctors and researchers to focus their resources on other key aspects of trial management and development. This is particularly beneficial as clinical trials become more complex and CRO’s are required to coordinate large scale patient numbers, randomization, supply distribution and inventory management. Cryosite can now provide pharmaceutical companies and their CRO’s with a scientifically trained logistics team that can streamline day to day trial logistics including inventory management, movement of trial supplies including drugs, case report forms, and returns, certified destruction and reconciliation both during and at the end of a particular study.

Operations are carried out in a state-of-the-art 800m² NATA accredited (ISO/IEC 17025) facility and in compliance with current Good Manufacturing Practices (cGMP). Our facility is secured and monitored 24 hours a day and provides clients with monitored and controlled ambient, chilled and low temperature storage options. Our Quality Assurance (QA) ensures compliance with all necessary regulations and detailed document control. All staff have formal scientific qualifications and understand the high level of importance that needs to be associated with your samples.