Clinical trials are a part of healthcare research and development that test the viability of the medication introduced newly, before making it available for public consumption in the market. However, trials can only be conducted on people who are interested, eligible based on certain criteria, and consent to the possible risks. Through this process, the medical history of the eligible person is reviewed, consent is obtained, and coordinated with researchers, ethics committees, and other regulatory bodies. To manage the complete process, the clinical trial participation approval process is used.

The traditional way of handling the trial participation approval process is manual and paper-based. This often leads to errors and multiple rounds of approvals, consuming a longer time to get the requests approved. This will delay patient enrollment and create compliance issues. 

This is why automating the clinical trial participation approval process is ideal. This will help streamline the different tasks and tackle the challenges that put down the efficiency of the process. From the request creation to the final approval, the tool offers auto-verification, compliance checks, routing, and approval. This enhances the accuracy of approving eligible people for clinical trials.