The IVDR transition includes structured processes IVD manufacturers must follow to engage with Notified Bodies. Many IVD manufacturers are interacting with Notified Bodies for the first time and must understand what is required to ensure a successful partnership. In this article, Dr. Oliver Eikenberg clarifies what manufacturers must prepare and when to engage a Notified Body for IVDR CE Marking.
An overview of essential human factors engineering standards and guidance for global medical device manufacturers.
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A guide to regulatory clearances, global reimbursement strategies, and the essential PICO approach.
Whether looking for more information or ready to partner with us, we're here to guide you through every step of the regulatory process.