Description

In the highly regulated world of medical devices, design controls are not just a mandatory step in your go-to-market journey; they are pivotal in driving product quality and safety. 

This webinar goes beyond the basics to provide a comprehensive deep dive into design controls, tailored to the unique challenges faced by premarket medical device companies. 

You’ll learn how you can leverage design controls to enhance product development, streamline compliance, and mitigate risks. 

During this presentation, we will identify the optimal stages in your development process to integrate design controls for maximum impact, explore practical applications of design controls within your organization, and analyze case studies that demonstrate the financial and safety repercussions of noncompliance. 

Key Takeaways 

• Understanding of design controls throughout the product lifecycle 
• Differentiation between design controls and change control mechanisms 
• Insight into the impact of noncompliance on patient safety and manufacturing costs 
• Strategic timing for implementing design controls 
• Practical guidance on employing design controls to enhance product development

Speaker

• Eric Bash, Senior Manager, Design and Development Quality Engineering at Gilero a Sanner Group Company 

REGISTER HERE