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In this episode of MedTech Global Insights, we challenge the traditional, fragmented approach to regulatory consulting that often leaves MedTech and IVD companies struggling with delays, duplicated work, and inconsistent strategies across different markets. We explore the limitations of hiring multiple local consultants and introduce a modern, integrated alternative for achieving rapid and compliant global expansion. We delve into the evolution of regulatory affairs, moving beyond the old model to a unified, technology-driven platform. Discover how a "single process, multiple markets" strategy, powered by AI and a global network of local experts, is becoming the new industry standard for companies looking to scale efficiently and predictably. What You'll Learn: Why is the traditional, country-by-country consulting model becoming obsolete for fast-growing MedTech firms? How can a "single process, multiple markets" strategy dramatically reduce your time to market? What role does Artificial Intelligence play in streamlining technical dossier submissions today? Is it possible to have a single point of contact for regulatory access in over 30 countries? How do you select the best international markets for your device without spending a fortune on research? What are the hidden costs of using disconnected local regulatory agents? How can integrated post-market surveillance across multiple regions protect your company from compliance risks? Contact us at [email protected] or visit https://pureglobal.com/ to learn more.