Upcoming Webinar: Designing for Safety: How Quality, Risk, and Patient Impact Interconnect

Medical device development requires a comprehensive understanding of how quality systems, risk management, and patient safety work together throughout the product lifecycle.

👉🏽 Register now!

As regulatory frameworks increasingly emphasize patient-centric approaches, manufacturers must move beyond compliance checklists to create integrated safety strategies that anticipate and mitigate real-world risks.

Join us on August 19, 2025, for "Designing for Safety: How Quality, Risk, and Patient Impact Interconnect," where we'll explore how to build robust safety frameworks that protect patients while supporting business objectives.

We will focus on:

• Integrating risk management principles into quality system design from concept to post-market
• Identifying critical connection points between quality processes and patient safety outcomes
• Developing proactive risk assessment strategies that go beyond regulatory minimums
• Creating feedback loops that continuously improve safety performance based on real-world evidence

Who should attend:

• Quality professionals responsible for risk management implementation
• Regulatory Affairs teams developing safety documentation
• Medical Device manufacturers seeking to enhance their safety culture
• Risk management specialists working on patient impact assessments
• Teams transitioning from reactive to proactive safety approaches

With Subject Matter Experts: 

• Andrew Gibson, PhD, Senior Managing Consultant and Team Leader, AKRA TEAM
• Arie Henkin, Chief Clinical Officer, Omniscient Neurotechnology (o8t)
• Notified Body Speaker (TBA)

Date: August 19, 2025 Time: 4 PM CET / 10 AM ET*

*Recording and slides available to all registrants

This session offers practical guidance on developing integrated safety strategies that safeguard patients while promoting regulatory compliance and business success.

👉🏽 Register now!