Navigating the FDA's Medical Device Reporting (MDR) regulation, 21 CFR Part 803, is a high-stakes requirement for any MedTech company in the US market. A single misstep in reporting an adverse event can lead to warning letters, product recalls, and significant delays in future approvals. This episode provides a practical guide to understanding your obligations. We break down the essential questions: Who needs to report, what events are reportable, and what are the critical 5-day and 30-day deadlines. We explore the nuanced definitions of "serious injury" and "malfunction," which are common points of failure for many manufacturers, and discuss how to establish a bulletproof internal process for capturing and evaluating potential events from all sources. Consider this scenario: A startup's new monitoring device is implicated in an incident that leads to a patient's extended hospital stay. The internal team is unsure if it meets the FDA's definition of a "serious injury." The 30-day clock is ticking. A wrong decision could attract FDA scrutiny and jeopardize their next round of funding. This is the exact type of high-pressure situation we dissect in this episode. 本期干货 - What is the precise difference between a device 'malfunction' and a 'serious injury' in the FDA's eyes? - When does the 5-day reporting clock really start for your company after an event? - Are you required to report an incident if your device only *might* have contributed to it? - How can you avoid the most common documentation mistakes that lead to FDA Warning Letters? - What is the eMDR system, and are you using it correctly for all submissions? - Can a single reporting mistake in the US impact your market access in Europe or Asia? - How do you determine if a similar event that happened outside the US is reportable to the FDA? - What kind of training should your customer service and sales teams have to identify potential adverse events? For more information, contact us at [email protected] or visit https://pureglobal.com/