# Postmarket Surveillance of AI Systems: Proactive methods for identifying risk and improving product quality

December 13, 2023

,

4:00 pm

EST

30

mins

Recorded on

December 13, 2023

30

mins

This webinar provides actionable insights on navigating the post-market regulatory landscape and creating a process focused on patient safety for AI-enabled medical devices. It will focus on best practices, emerging threats, and the role of regulatory agencies in safeguarding data privacy and ensuring device security.

## What you'll learn

- **Build a more efficient AI post-market surveillance with best practices and modern tools:** Explore best practices for post-market surveillance to optimize AI devices for safer, more reliable outcomes.
- **Achieve regulatory success in Adaptive AI:** Learn to navigate the intersection between post-market surveillance and regulatory requirements by addressing ongoing challenges for AI development and those trying to regulate it.
- **Prioritize safety by knowing when and how to engage with regulatory authorities for AI-related modifications:** Understand at what point a modification to an AI device requires resubmission for FDA approval and how to communicate with regulatory authorities throughout the process.

## Who should attend

- Research and development teams
- Regulatory affairs and compliance personnel
- Software development teams

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### Clips from this Webinar

## Speakers

### Erez Kaminski

Founder & CEO

[Ketryx](https://www.ketryx.com/)

Formerly

## Interested?

[Register now](https://www.ketryx.com/learn/webinars/register/postmarket-surveillance-of-ai-systems-proactive-methods-for-identifying-risk-and-improving-product-quality#register)