Here is a list of upcoming webinars for the medical device industry. Subscribe to The Medical Device Broadcast newsletter by clicking here
Medtech Development – From Concept to Market
Date: Sep 25, 2025
Time: 12 PM ET
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Get life-saving medical devices into the hands of surgeons and patients faster and more efficiently. Currently, three quarters of medtech innovations fail to make it to market. Archetype’s Dr. Stuart Grant, PhD, principal consultant and medtech visionary, will discuss how a comprehensive suite of services embeds market approval into the DNA of the medtech product design innovation process. Learn why integrating market approval into every stage of product development is necessary to streamline the concept to market process for successful product launches.
Eurofins: Navigating the Shift from Automotive to Medical Device Quality Standards
Date: 25 September, 2025
Time: 09:00 AM ET
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In this one-hour webinar, we will explore:
- The key differences between ISO 9001 and ISO 13485
- Regulatory and quality management implications of the transition
- Common challenges and pitfalls during implementation
- Practical strategies for a smooth and compliant migration
MDIC: Translating New Regulation into Actionable Risk Management Strategy
Date: 30 September, 2025
Time: 03:00 PM ET
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This one-hour virtual event features an expert panel discussion followed by a live Q&A session. Hear directly from leaders across quality, insurance, technology, and standards development as they explore the future of risk management and how to prepare for the 2026 compliance deadline.
Intro to Medical Device Submission – 510(k)s, PMAs & Exemptions
October 9, 2025
12:00-15:00 EDT
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This webinar will discuss current US Federal law on the 510(k), IDE, DeNovo, and PMA and associated requirements for getting a new or substantially changed medical device through the US FDA review process and to market in the USA.