Join us at the , April 4-6, 2022, in Pacific Grove, CA.
Learn how ºÚÁϲ»´òìÈ can provide the data you need to ensure your cardiac and endovascular devices receive regulatory approval for use. Visit us during the event or request a meeting below. We'd love to discuss how ºÚÁϲ»´òìÈ's testing expertise can help keep your project on track.
About the event
This event is intended to link anatomic and physiological conditions to implant design and to the engineering mechanics of fracture. CVID brings together experts in the fields of medicine, biomechanics, computational analysis, and engineering testing from the medical device industry, academia, physicians and regulatory agencies.
Book a meeting
Schedule a meeting with one of our experts to learn more about how we can help you to develop better products, save time and money, and minimize potential risk to your business.
Learn more
Cardiovascular Device Testing
ºÚÁϲ»´òìÈ specializes in a wide range of testing for cardiovascular devices, such as stents, grafts, occluders, catheters, heart valves and pacemaker leads.
On-Demand Webinar: Testing Stents and Other Cardiovascular Devices
In this on-demand webinar, Scott Anderson, P.E., discusses the regulatory standards and an overview of relevant testing methods for cardiovascular devices.
Medical Device Regulatory Services
ºÚÁϲ»´òìÈ’s regulatory advisors have 30 years of domestic and international regulatory consulting experience, specializing in handling the most complex challenges and partnering with you on the path to submission.Â
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