Created by a team with in-depth experience of the UK clinical research sector, TCRS provides a full range of clinical development services to pharmaceutical companies, biotechnology organisations and university academics.
Having previously held senior posts within the NHS and academia, we are uniquely qualified to offer guidance on the UK’s legislative framework, and give advice on designing protocols to meet UK Regulations.
Working closely with the National Institute of Health Research, we can use real data to rapidly identify the most suitable UK sites for your category of study and therapeutic field.
We had a key role in developing the new HRA system for study approvals making us ideally qualified to help you to navigate this new and sometimes challenging process.
Whether you are seeking support for every aspect of your clinical research project or are looking to outsource just one part of a study, we bring a focused approach that complements our in-depth knowledge.
We understand that every study is different and every sponsor has different priorities – our services are tailored to your specific requirements.
With established relationships to key personnel and sites across the UK clinical research field, TCRS offers flexibility, momentum and value.
Our network of Senior CRAs and Project Managers across Europe, and strategic partners in the USA and Australia, enable TCRS to offer global reach coupled with a lean and highly cost effective infrastructure.
Long-standing relationships with international regulatory authorities, ethical bodies and senior clinicians ensure that site selection, set-up and management is conducted with optimal efficiency wherever it is required.
We understand that the quality of project delivery is critical for success. For this reason our international service is underpinned by rigorously controlled quality management, recruitment and training systems. It is overseen by a highly experienced management team.