In the race for global market access, the biggest hurdle isn't always the regulations themselves, but the 24-hour clock. When your teams are spread across continents, progress can grind to a halt while one part of the world is asleep, turning simple questions into 48-hour delays. This episode dives into the hidden operational drag of time zone differences in MedTech regulatory affairs. We explore why the traditional model of hiring separate local consultants is no longer sufficient in a hyper-connected world. We'll show you how a unified, "follow-the-sun" approach, powered by local experts in a single global team, can transform your expansion strategy from a series of stops and starts into a continuous, 24/7 operation. --- **Case In Point:** A German MedTech company's expansion into the US and Brazil was crippled by communication lags. A simple technical query to their FDA consultant took two days for a response, while the Brazilian submission waited on that feedback. We break down how this common scenario creates friction, multiplies costs, and jeopardizes launch timelines. --- **What You'll Learn:** * What is the true cost of the "24-hour time lag" in a global product launch? * How can a simple question between your EU and US teams lead to a 48-hour project delay? * Why is the traditional model of hiring separate in-country consultants failing MedTech scaleups? * What does a "follow-the-sun" regulatory workflow look like in practice? * How can one unified process get you market access in over 30 countries without the logistical nightmare? * What is the key advantage of having local experts who are part of a single, global company? * How does a centralized data platform prevent information silos between your teams in Asia, Europe, and the Americas? --- Contact us at [email protected] or visit https://pureglobal.com/