Clinical trials are an essential part of the development of new medical treatments and procedures, and they help to ensure that new interventions are safe and effective for patients above all. Because of that, it is really important that all steps in that process were done with special attention to patient safety above all, but also to the accuracy of data that is often still collected manually, which slows down the entire process, and sometimes even compromises it, which result with the fact that clinical trials are exposed to frequent audits precisely for this reason.

Although clinical trials are essential for advancing medical knowledge and improving patient outcomes, there are several challenges associated with the current approach to conducting trials, including high costs, slow recruitment, lack of diversity, regulatory burden, data management challenges, and lack of transparency. Addressing these challenges will be essential for improving the efficiency and effectiveness of clinical trials in the future.