In Vitro Medical Device Regulation Roadmap (IVDR)

New In Vitro Device Regulation (IVDR)
Duration:  Unlimited
Cost:  49  USD
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This course describes general principles and gives practical advices on how to plan and prepare for the IVDR.
In this course, we will cover all the necessary regulatory references. We will discuss in details an article 56 of IVDR. Moreover, you will learn about general safety and performance requirements. We will also explain what is the performance evaluation and step by step we will guide you through its components. At the end, we will highlight your periodic deliverables so you will be aware on what and when needs to be updated.
Length: 00:20