Navigate the Global Audit Landscape with ConfidenceEducation Sessions<img alt="" height="200" src="https://assets.swoogo.com/uploads/medium/3515333-65c26100c2dd2.jpg" style="margin:10px;float:right;" width="300" /> The medical device industry faces a dynamic audit environment with increasing scrutiny from regulatory bodies worldwide. This session empowers you to confidently navigate the complex audit landscape and ensure successful outcomes. Join industry experts for an in-depth exploration of the drivers behind the surge in audits from FDA, EU and other key regulatory authorities. You’ll also learn how to demystify factors influencing your audit probability, including the impact of quality certifications like ISO 13485 and MDSAP. Discover proven strategies to proactively manage and optimize your audit experience, minimize risks and ensure compliance. Learn how to navigate the specific requirements and expectations of FDA, EU and other regulators to ensure preparedness for global audits. During the interactive panel discussion, you’ll engage with seasoned professionals and fellow attendees to share best practices, ask questions and build a stronger audit preparedness network. Don’t be overwhelmed by the ever-changing audit landscape. Equip yourself with the knowledge, strategies and connections you need to navigate audits confidently and ensure the success of your medical device journey. This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.

Description

The medical device industry faces a dynamic audit environment with increasing scrutiny from regulatory bodies worldwide. This session empowers you to confidently navigate the complex audit landscape and ensure successful outcomes.

Join industry experts for an in-depth exploration of the drivers behind the surge in audits from FDA, EU and other key regulatory authorities. You’ll also learn how to demystify factors influencing your audit probability, including the impact of quality certifications like ISO 13485 and MDSAP. Discover proven strategies to proactively manage and optimize your audit experience, minimize risks and ensure compliance. Learn how to navigate the specific requirements and expectations of FDA, EU and other regulators to ensure preparedness for global audits. During the interactive panel discussion, you’ll engage with seasoned professionals and fellow attendees to share best practices, ask questions and build a stronger audit preparedness network.

Don’t be overwhelmed by the ever-changing audit landscape. Equip yourself with the knowledge, strategies and connections you need to navigate audits confidently and ensure the success of your medical device journey.

This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.