『Unlocking Global Markets for Orthopedic Implants: A Pure Global Guide to Navigating FDA, CE, and Emerging Market Regulations』のカバーアート

Unlocking Global Markets for Orthopedic Implants: A Pure Global Guide to Navigating FDA, CE, and Emerging Market Regulations

Unlocking Global Markets for Orthopedic Implants: A Pure Global Guide to Navigating FDA, CE, and Emerging Market Regulations

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 In this episode of MedTech Global Insights, we explore the rapidly growing orthopedic implant market and the immense regulatory challenges that manufacturers face. With an aging global population driving demand for devices like knee, hip, and spinal implants, the path to international market access has never been more complex. We break down the specific hurdles in key regions, from the stringent clinical evidence requirements of the EU's MDR to the nuanced 510(k) pathway of the US FDA. We also examine the unique difficulties in emerging markets across Asia and Latin America, where local regulations can create significant delays. This episode provides a strategic roadmap for overcoming these obstacles through an integrated, technology-driven approach. A real-world example. a European scaleup developed an innovative spinal cage. They achieved CE marking but then hit a wall. Their plans to launch in Brazil, South Korea, and Mexico simultaneously were stalled by conflicting requirements, language barriers, and the need to find a separate local representative for each country, delaying their expansion by over 18 months. In this episode, you will learn the answers to these questions: - Why has the EU MDR become the biggest regulatory challenge for orthopedic implant manufacturers? - What are the critical differences in clinical data requirements between the US FDA and European authorities? - How can you leverage a single technical dossier to gain access to over 30 global markets simultaneously? - What are the hidden costs and delays when registering devices in key emerging markets? - How can AI technology dramatically accelerate the compilation and submission of your regulatory documents? - What specific post-market surveillance activities are now mandatory for orthopedic devices in Europe? - How do you select the right international markets for your product to maximize ROI on regulatory spending? Contact us for more information at info@pureglobal.com or visit https://pureglobal.com/
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