The contribution of medical research in improving the quality of healthcare provided to patients is pivotal. All medical research proposals go through a lengthy and stringent review process before being approved. In this process multiple stakeholders from various departments are involved. With such high stakes associated with approval of medical research papers, manual workflows are inadequate. 

Only when research work is approved on time can research timelines be accelerated and compliance be enhanced. So, to derive maximum benefit out of medical research work, it is important that the review and approval process is carried out efficiently. The best way to achieve this is to adopt workflow automation with a no code solution like Cflow. With the review and approval process automated, all research work is accurate and compliant with regulatory policies. Moreover, automated systems ensure that the requests are routed to the appropriate stakeholder for review, which accelerates the approval process and improves the coordination between teams.