Our team at Sitilop has significant experience in conducting clinical trials and developing study protocols tailored towards the needs and objectives of the sponsor.

We work closely with sponsors to develop a protocol that will meet the highest scientific and clinical standards and prepare the synopsis, the schedule of activities, the abstract; the primary, secondary and exploratory outcome measures as needed, the study design, inclusion and exclusion criteria, the statistics and sample size calculation, study and data management, the dissemination of Results, the adverse events and study conduct considerations, among others.

Our team specialises in the review of study protocols and the assessment of study feasibility. For example, we can identify potential problems impacting study execution and recruitment and retention. We can advise on selecting the best locations to conduct the study on the basis of clinical and research facilities, recruitment targets, competing studies and funding; and we can advise on recruitment strategies. In Sitilop we can also offer specialised guidance and recommendations, and precise execution with solutions for roadblocks in order to ensure timely study execution.

Meet our team

Our vision is to drive healthcare forward, and accelerate this progress with our unique insights, and with our ability to reimagine and reinvent. Our team is constantly striving to innovate and find novel solutions to provide state-of-the-art services, in all aspects of clinical research, ranging from clinical activities, to the establishment of research protocols, regulatory and ethics submission, data analysis, using innovative and novel methodological approaches, and preparing materials for publication.