Post by GMED

📅 July 2026 Virtual Trainings | Strengthen Your Regulatory & Compliance Expertise Whether you're preparing technical documentation, enhancing product safety, or strengthening your post-market processes, GMED North America's July training program delivers practical knowledge from experts who assess medical devices every day. 🔹 July 14–15 | Technical Documentation per MDR (EU) 2017/745 Build compliant MDR technical documentation and understand notified body expectations throughout the conformity assessment process. 🔹 July 14–15 | Technical Documentation per IVDR (EU) 2017/746 Develop robust IVDR technical files and gain insights into common challenges, documentation gaps, and best practices. 🔹 July 21–22 | Medical Device Electrical Safety Strengthen your understanding of electrical safety requirements and their application to medical device design, testing, and compliance. 🔹 July 28 | Post-Market Surveillance & Vigilance Learn how to establish effective PMS processes, manage vigilance obligations, and leverage post-market data to support ongoing compliance. 🎯 Whether you're focused on MDR, IVDR, product safety, or lifecycle compliance, these sessions provide actionable guidance to help you navigate today's evolving regulatory landscape. 👉 Register here: https://lnkd.in/eNxSgUeq 💡 First-time participant? Returning attendee? Registering multiple colleagues? Special rates may apply. Contact us at [email protected] to learn more about available first-time, loyalty, and group discounts. #MedicalDevices #IVDR #MDR #TechnicalDocumentation #PostMarketSurveillance #Vigilance #ElectricalSafety #ISO13485 #RegulatoryAffairs #MedicalDeviceTraining #IVD #GMEDNorthAmerica