What is ViSU?
ViSU is a Regulatory & Product Submission Platform from DDI. Our innovative RIM solutions are designed to streamline the submissions process and speed up time-to-market, while also improving communication with regulators and maximizing your research investments. Say goodbye to long cycle times and hello to increased value for your business.
ViSU: Your Solution for Effective Regulatory Management for Medical Device Organizations.
ViSU is aRegulatory Information Management System that allows medical device organizations to effectively manage regulatory audits and keep up with the ever-changing requirements of new markets. Without a robust RIMS like ViSU, organizations may face various challenges including longer document compilation and application submission times, resulting in delayed approvals and revenue loss. Additionally, ViSU helps to minimize compliance costs, especially with impending regulations such as the EU MDR and IVDR. ViSU also provides direct reporting capabilities, giving senior management full visibility and eliminating blind spots within the organization. Don't let regulatory complexities hinder your success, choose ViSU for efficient and streamlined regulatory management.
