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 what can, at times, be a 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.