Clinical Evaluation and PMS: Using Interfaces in Practice - For professionals who would like to familiarise themselves with current requirements and future changes

"Both clinical evaluation (CE) and PMS are mandatory for every medical device manufacturer in Europe regardless of the risk class. The clinical evaluation can trigger a PMCF, which is a central and critical component of market surveillance, especially if the original conformity assessment procedure was exclusively based on equivalent products. This comprehensive online course addresses the importance of clinical evaluation, PMS and the PMCF, as well as the associated vigilance and market surveillance in terms of Regulation (EU) 2017/745 (MDR) in the course of two mornings. Our experts will discuss the current legal framework and requirements for clinical evaluation and PMS, and guide you on how to successfully comply with the complex regulations in practice."