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UID:6a3fab76ee52e@gha.health
DTSTAMP:20260627T105238Z
DTSTART:20260617T160024
DTEND:-00011130T170024
SUMMARY:Online Panel Discussion: Navigating Regulatory Approval for Medical Devices
LOCATION:Online
DESCRIPTION:Regulatory approval is the final and most critical step before launching a medical device — but getting there efficiently is becoming increasingly complex.\n\nIn this upcoming webinar, UL Solutions experts will explore how manufacturers can navigate global regulatory requirements more effectively, with a focus on medical device cybersecurity, electrical safety and certification strategies.*\nKey takeaways\nDuring the webinar, UL Solutions experts will discuss key questions and practical considerations for medical device manufacturers preparing for compliance, such as:\n\n 	How can medical device regulatory requirements be met efficiently before launch?\n 	Is there a single global standard for medical device cybersecurity?\n 	Are electrical safety requirements still a real challenge — or just a formality?\n 	How can manufacturers achieve global compliance faster and at lower cost?\n 	Do regulators prefer certified results over standalone test reports?\n\n \n\nTo register, please follow the link below:\n\nOnline Panel Discussion: Navigating Regulatory Approval for Medical Devices | UL Solutions (https://www.ul.com/events/online-panel-discussion-navigating-regulatory-approval-medical-devices?utm_source=linkedin&utm_medium=social&utm_campaign=medtest_medicaltesting_bf&utm_term=cmit&linkId=942341845)
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