[WEBINAR] How to navigate the EU MDR requirements for Clinical Evaluation

HOW TO NAVIGATE THE EU MDR REQUIREMENTS FOR CLINICAL EVALUATION

 

Professionals in the MedTech industry know that Clinical Evaluation is a key process that must be performed for all types of medical devices. However, a lot of manufacturers still struggle with navigating the related requirements and defining the level of clinical evidence necessary to demonstrate conformity with the regulatory frameworks.

 

In this recorded webinar, Sofia Spjuth from Veranex/Devicia and Dr. Johannes Leidner from Medidee/Veranex share key stages of the clinical evaluation process and provide insights and experiences related to some hot topics including but not limited to:

  • Clinical Evaluation Strategy
  • Safety and Performance Parameters
  • Data appraisal
  • Post-Market Clinical Follow-up
  • Clinical Evaluation of Medical Device Software (MDSW)

 

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