The 2nd Annual Outsourcing in Clinical Trials: Medical Devices USA brings together clinical, regulatory, and commercial leaders from across the medical device and diagnostics community for two days of insight and networking in Minneapolis. Sessions cover FDA and EU MDR regulatory updates, AI in clinical operations, decentralized trial design, cybersecurity evidence requirements, and post-market surveillance strategy.
Meet us thereNavigate FDA and EU MDR regulatory pathways with confidence
Leverage AI and digital tools in clinical operations
Design and execute decentralized trials for devices and IVDs
Build robust post-market surveillance and cybersecurity evidence
Stop by booth 11 to speak with our clinical and regulatory experts about your device strategy.
Our QbD Clinical experts will be on the floor. Schedule a meeting ahead of the event to discuss your clinical trial strategy for medical devices and IVDs.
Let our experts help you navigate the complexities of life sciences regulation and quality.
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