We review and critically evaluate the published literature to write protocols for large CROs and academic institutions.
Our highly trained researchers have academic degrees and can provide tailored clinical trial design for your project.
We work with research ethics, scientific and medical advisory boards to manage and submit your clinical trials to ethics, scientific and data committees.
We merge real-world evidence and patient experience in clinical trial design for a more personalised approach.
We provide data, independent audits and quality assurance systems to control data collection, analysis, and reporting.
We collaborate with industry, academics and researchers to bring new treatments to patients.