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For medical device manufacturers, responding to new regulations and standards is of utmost importance, but researching the latest information from various sites and tools is a challenging task. By using the Compliance Navigator, you can simply register relevant regulations and standards in product-specific folders, and when there are changes or planned revisions, the entire team can receive notification emails and immediately refer to the content online. Additionally, it includes numerous revision history versions that clearly show the differences between old and new standards, as well as expert explanations to support correct interpretations. In this webinar, we will provide a detailed introduction to how the Compliance Navigator can assist in complying with medical device regulations, while viewing actual system screens.