In the medical device industry, conducting thorough and compliant Clinical Evaluations is a critical part of ensuring the safety and effectiveness of your products. At meddevo, we've developed eCER, an automated solution for Clinical Evaluations, designed to dramatically reduce the effort required to create and update these crucial documents.
Our eCER software offers an automated solution for Clinical Evaluations. It allows you to create and update your Clinical Evaluation documents with ease. With eCER, you can automate the creation and update of CEP, CER, and many more, ensuring your documents are always up-to-date.
With eCER, your Clinical Evaluation content no longer has to be laboriously picked out and copied from the technical documentation. Our software automatically populates itself with the information from the eTD, saving you time and reducing the risk of errors.
Based on the meddevo eTD standard eCER serves as a single source of truth for your Clinical Evaluations. With shared content and no redundancy, eCER keeps your documentation clean and organized. It also ensures that you never forget to revise your documents, reducing the risk of non-compliance.
Our software promotes collaboration and process automation, making it easier for your team to work together and stay on the same page. With eCER, you can streamline your Clinical Evaluation process, improve efficiency, and ensure that your medical devices meet the highest standards of safety and effectiveness.
Ready to experience the future of Clinical Evaluations? Learn more about eCER and discover how our software can streamline your Clinical Evaluation process.
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