
16th Annual
IVD Clinical & Regulatory Affairs Conference
December 2022 | Chicago, IL
Optimize Submission Strategies to Secure Approval from Global Regulatory Authorities for Innovative & Existing Products
Program Overview
As global regulations change, IVD manufacturers must adapt to a vastly different regulatory environment. The swiftly approaching EU IVDR has created a challenge for regulatory and clinical affairs professionals in the diagnostic space, as companies must find harmony between the multitude of different regulations in the EU, UK, Switzerland, Canada, China, and the US. Additionally, cybersecurity breaches have become a major focal point for the diagnostic industry, as different countries have created new regulations to maintain cybersecurity standards. With quality case studies and panel discussions regarding global regulatory changes and compliance strategies, the 16th Annual IVD Clinical & Regulatory Affairs Conference will continue to deliver a first-in-class educational and networking platform for diagnostic regulatory and clinical affairs executives.
Q1 PRODUCTIONS SAFEGUARD
As we welcome you back to our in-person conferences and forums, we want to assure you that providing a safe and comfortable environment in which to learn is of paramount importance to us. For the safety of all attendees, Q1 Productions will follow COVID-19 protocols to comply with CDC guidelines, state and local regulations. To learn about Q1 Productions SAFEGUARD, please click here.
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An exclusive experience with professional thought leaders provides you with direct insight into current solutions.

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Learn through dynamic panel discussions, case studies and real world evidence on current topics directly related to your industry.

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Chris Cockerell
Senior Event Manager
Q1 Productions
+1 (312) 224-8722
ccockerell@q1productions.com
www.q1productions.com