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The International Medical Device Regulators Forum (IMDRF) has just released a new final document!
This latest document, IMDRF/GRRP WG/N71, is part of a series aimed at streamlining the regulatory approval process for medical devices. Building upon existing guidelines, it focuses on the crucial aspect of regulatory review reports.
By specifying the information that should be included in these reports, IMDRF/GRRP WG/N71 ensures a standardized approach across regulatory jurisdictions. This not only promotes efficiency but also enhances collaboration between review bodies and regulatory authorities.
At Medical Devices Regulatory — support unit (MDRu) we understand the importance of staying up-to-date with regulatory updates like IMDRF/GRRP WG/N71. Visit our website to learn more about how we can assist you in navigating these changes and ensuring compliance with regulatory requirements: https://lnkd.in/dt4tQYNy
Let’s work together to drive innovation while maintaining the highest standards of safety and performance in the medical device industry!