Скачать или смотреть Scaling MedTech Startups Through FDA and Common Mistakes | AdvaMed San Diego 2025

FDA approval is the gateway to market success for MedTech startups, but navigating regulatory requirements from prototype to commercialization requires strategic planning, realistic timelines, and expert guidance. In this exclusive interview from the MedTech World at AdvaMed's MedTech Conference, Mridul Mittal from Mittal Consulting shares insider knowledge on regulatory strategy, common pitfalls, and how startups can move faster through the FDA approval process.

Discover why most MedTech startups underestimate regulatory timelines, how to avoid tunnel vision about product-market fit, and why FDA approval is more cost-effective and efficient than EU MDR for medical device companies seeking global market access.
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