EU MDR & IVDR Certification: Navigating the Notified Body Capacity Crunch and Timeline Compression

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EU MDR & IVDR Certification: Navigating the Notified Body Capacity Crunch and Timeline Compression

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This episode delves into the ongoing Notified Body capacity crisis for EU MDR and IVDR certification. Despite extended transition deadlines, significant bottlenecks in audit scheduling and technical documentation review are creating a "timeline compression" risk. We explore why manufacturers must strategically prioritize their product portfolios and engage with Notified Bodies much earlier than planned to avoid jeopardizing market access as deadlines approach. - Why is Notified Body availability still a major risk despite MDR/IVDR deadline extensions? - What is "timeline compression" and how does it affect legacy devices? - How should manufacturers strategically prioritize products for EU certification? - What are the hidden delays in scheduling audits and technical file reviews? - Was the May 26, 2024 application deadline a false finish line? - Are the extended transition periods creating a false sense of security? - What steps can you take now to secure your place in the certification queue? Pure Global provides end-to-end regulatory consulting for MedTech and IVD companies, leveraging local expertise and advanced AI to accelerate global market access. We develop efficient regulatory strategies, assist with technical dossier submissions, and act as your local representative in over 30 markets to get your products approved efficiently. Our technology-driven approach streamlines compliance and market research, helping you navigate complex environments like the EU. Whether you are a startup or a multinational, we have scalable solutions to support your expansion. Contact us at info@pureglobal.com, visit https://pureglobal.com/, or explore our FREE AI tools and database at https://pureglobal.ai.

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