The set up process and ongoing continued monitoring of clinical trials and medical device studies is the bedrock of our business. Covering the process from study conception right through to project completion, our team are highly skilled at all facets of the clinical trials and medical device studies process.
From evaluating the suitability of investigators and their sites (see section 5), through site set up and patient recruitment, to the clinical monitoring process and finally the completion and closure of the trial on site, our team is highly experienced at managing the clinical trials and medical device study process at all phases of the development life-cycle. If required, we can have as much input as desired on aspects such as the monitoring plan and report structure. We have much experience within monitoring and are extremely well-placed to advise on the best practise, tailored perfectly to your individual needs.