Developing safe, innovative, market-ready medical devices requires answering a range of tough questions throughout the product lifecycle:
- How can we meet FDA wear testing and biotribology requirements?
- What testing will we need if we change materials for our next-generation device?
- How can retrieval analysis help us revise our implantable medical device design?
- What standards should we use for MRI safety labeling?
- And more.
At the ORTHOmaterials Orthopeadic and Dental Devices Manufacturing Technology Forum in Changzhou, China, connect with Exponent's Shanghai office at booth 10 to learn about our extensive life sciences consulting services for medical device manufacturers. On Sept. 8, hear Mechanical Engineering Senior Manager Lijie Yang, Ph.D., present our medical device analysis and regulatory support capabilities and see what we can help you solve. More details below.
"Medical Device Analysis and Regulatory Support"
FRIDAY, SEPT. 8 | 9:40-10:20 A.M.
Speaker: Lijie Yang, Ph.D.
Exponent's life sciences consulting team consists of multidisciplinary engineers and scientists focused on solving engineering, science, regulatory, and business challenges facing the life sciences and medical device manufacturing industries at every stage.
This presentation will discuss how we can help support your medical device development through cutting-edge Finite Element Analysis for Medical Devices & Biomaterials, Retrieved Device & Tissue Analysis, testing for MRI Compatibility, evaluation of materials in medical devices and implants, and other services.