All day: The Future of QMS Requirements True Quality Summit Series
All day November 1, 2022 – November 2, 2022
What does the future hold for QMS requirements? Why are regulatory bodies changing requirements and what do they expect from your organization? Join us to learn from industry experts, including Francisco Vicenty from FDA, who will guide you through recent changes to QMS requirements, and share perspectives on where the industry could be headed in the future. Can't attend live? Register anyway and access all the information after the conference.
All day: The Future of QMS Requirements True Quality Summit Series
All day November 1, 2022 – November 2, 2022
What does the future hold for QMS requirements? Why are regulatory bodies changing requirements and what do they expect from your organization? Join us to learn from industry experts, including Francisco Vicenty from FDA, who will guide you through recent changes to QMS requirements, and share perspectives on where the industry could be headed in the future. Can't attend live? Register anyway and access all the information after the conference.
12:00 pm: Monetizing Software: The Challenges of Commercialization & How to Overcome them
12:00 pm – 1:00 pm November 3, 2022
If you currently have a consumables revenue stream, why not create a revenue stream out of medical device software? Be sure your organization is not missing out on revenue from the largest part of medical device product development – software!
Join us for a live webinar as industry experts Shawnnah Monterrey, CEO of BeanStock Ventures, Kate Burns, Senior Software Product Manager at Arthrex, and Chris DuPont, CEO of Galen Data, explore how you can tackle the challenges associated with commercialization and monetize your medical device software. Register for free today!
9:00 am: NAMSA Training Series: ISO 10993-18:2020 Chemical Characterization of Materials
9:00 am – 3:45 pm December 1, 2022
Join NAMSA’s team of testing experts as they lead a discussion on chemical characterization of materials and provide learning that will allow attendees to:
Relate ISO 10993-18:2020 to ISO 10993-1:2018 and the biological evaluation of devices
Discuss the changes in the new document in a practical use format
Discuss how material and chemical characterization fit into the MDR
Develop a testing strategy for multiple devices
Plan for future testing needs of materials and finished medical device
Solve problems that may occur during testing, such as a degraded sample or liquid test articles