Risk management is a cornerstone of medical device and IVD development. It's a complex process that requires meticulous attention to detail. That's where eRisk comes in. Our innovative software solution automates and syncs your risk management documents, freeing you to focus on what truly matters - analyzing and mitigating risks.
eRisk is designed to streamline your risk management process. It automatically populates risk management documents with data from your Clinical Evaluation, PMS and Technical Documentation, eliminating the need for manual data entry. This not only saves time but also ensures accuracy and consistency across your technical documentation.
With eRisk, you can automate the creation and update of your Risk Management Plan (RMP) and Risk Management Report (RMR). This means your documents will always be current, reducing the risk of non-compliance. Plus, with shared content and no redundancy, eRisk helps keep your technical documentation clean and organized.
eRisk fosters collaboration and process automation. It allows your team to work together seamlessly, ensuring everyone is on the same page. With eRisk, you can improve efficiency, enhance collaboration, and ensure your medical devices and IVDs adhere to the highest safety standards.
Are you ready to revolutionize your risk management process? Experience the power of automation with eRisk. Discover how our software can transform your risk management process.
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