Brecon offers a comprehensive service for clinical trials supplies. Each project is assigned a dedicated manager who will work to ensure that our service matches our customers’ expectations in every detail. The project manager provides a single point of contact to keep customers fully briefed on progress and to provide access to accurate status information at all times.
Our clinical trials services are managed by qualified professionals with extensive experience in clinical research and packaging. All our activities are performed by highly trained and dedicated staff.
Our team of QPs is available for the release of clinical supplies for use within Europe in accordance with the new EU legislation. With extensive experience working with overseas clients, especially those from the USA and Japan, we can react to our clients’ needs and help smooth the process of importing clinical trial supplies into the EU.
Extensive in-house labelling services include design and printing, and generation of randomisations and code breaks, all with multi-language capabilities.
With an increasing demand from our customers for guidance in the completion and submission of regulatory documentation, translation services or EU legal representation, Brecon has established a partnership with a specialist regulatory affairs consultancy to offer a fully comprehensive clinical trials service from a single point of contact.
However complex the study, Brecon has the expertise and facilities to meet our customers' requirements and adopts a flexible, tailored approach to each project
Our comprehensive clinical trial services are managed by qualified professionals with extensive experience in clinical research and the capacity and breadth of vision to react rapidly to changing circumstances. Attention to detail is paramount, with all trials following strict procedures compliant with GxP