TCRS provides a complete range of clinical research consulting services.
We have the expertise to support entire clinical development programmes, but are equally happy offering advice on how to optimise study set-up at a specific investigative site.
Our experience of conducting clinical studies within the NHS ensures that the strategy we propose will be practical and realistic as well as meeting the highest standards of quality.
We have a broad range of contacts with senior opinion leader clinicians across all therapeutic areas, enabling us to provide definitive expert input on pharmaceutical products and medical devices.
Our Regulatory Affairs specialists will apply many years experience to develop a strategy tailored to the requirements of authorities in Europe, the USA and worldwide. Personal contacts within the agencies make us ideally placed to accompany our sponsors to meetings with the regulators.
We provide strategic statistical input in collaboration with our partners dataMagik. Further details are given in the “Data Management and Statistics” section of the website.
To assist with the study planning process we can also provide detailed study costings using project metrics derived from real-world experience of conducting clinical trials.
As a first step we would be happy to produce a “ballpark” costing free of charge.
If you require more comprehensive information, we can also provide costings for multiple project scenarios and a detailed analysis of the key cost drivers.