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Presented by: Grace Powers, Founder & Principal Consultant, Powers Regulatory Consulting

Join us for a session on regulatory strategy aimed at helping innovators understand the key considerations for determining the regulatory pathway for medical devices. This introductory session is designed for entrepreneurs new to medical device regulatory affairs who want to learn more about the requirements for bringing products to market.

Several important topics will be covered, including:

• Defining what constitutes a medical device
• A review of the basics of device classification
• Identifying the different types of pre-market submissions
• Describing the steps to bring a new product to market successfully
• Don’t miss out on this opportunity to learn from a pro!

This is the seventh session of the 2024-2025 Bench2Market series, which was created to provide commercialization guidance to the university research community. For more details on the series and the full schedule, visit the Biolocity website.

Check out our YouTube channel to watch previous webinars.