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text: "Regulatory Pathways you can use: A Hands-on Workshop for Novel Medical Devices." BioNext, Health Canada and FDA logos.

Medical Device Regulatory Pathways You Can Use

Join BioNext on February 25 for a hands-on workshop with Liz Munro (LMC Inc.), an expert in guiding medical device startups through FDA clearance. This session cuts through the jargon to provide a practical roadmap for US and Canadian market entry, covering device classification, early-stage prep, and aligning product milestones with regulatory demands. Get the actionable insights you need to move your tech to market at speed. This event is free and all are welcome to attend—snacks and refreshments will be provided!