Navigating Clinical Evaluation Excellence: A Strategic Guide for Medical Devices - Celegence Webinar

This session will delve into the best practical regulatory practices, and proven methods of crafting a winning strategy for conducting clinical evaluations on medical devices. If you are involved in CER preparation or literature reviews in general, this is an opportunity to increase your understanding of the processes, best practices and potential pitfalls associated with them.

During this webinar, step by step, we’ll unveil the key components of building a robust Clinical Evaluation Report (CER), explore the treasure trove of internal and external data sources at your disposal, and shed light on the common areas closely scrutinized by Notified Bodies.

Webinar Learning Objectives
1. How to develop a comprehensive clinical evaluation strategy
2. How to master the art of data sourcing
3. How to harness technology for efficiency

Celegence – Regulatory Services and Solutions to Support the Medical Devices and Diagnostic Industry

Celegence offers regulatory solutions and services that are tailored to the needs of medical devices and In Vitro Diagnostics (IVD) manufacturers. The benefits of our solutions and services include clear visibility and control over diverse product portfolios, increased operational efficiency, lowered costs, and ongoing regulatory compliance.

To learn more about our cost-effective software solution, CAPTIS, dedicated to EU MDR/IVDR compliance, reach out to [email protected] or contact us online to schedule a demo: https://www.celegence.com/technology/...