Take Control: Medical Device Supply Chain Compliance
A focused session for Medical Device supply chain compliance professionals
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How medical device teams can prepare for regulatory change across procurement, risk, and compliance
Supply chain compliance for medical devices is no longer manageable with spreadsheets, one-time supplier declarations, or static technical files. Regulations such as EU MDR, REACH, expanding PFAS restrictions, and Extended Producer Responsibility are forcing manufacturers to answer deeper questions about device materials, chemical content, and supplier change control, and many are discovering they cannot.
Auditors and customers are no longer asking whether you have compliance data. They are asking how current it is, how you validate it, and how you enforce control when suppliers change. For medical device manufacturers, the gap between perceived compliance and defensible compliance is widening fast.
The key supply chain regulations medical device organization need to focus on in 2026
How leading procurement teams are operationalizing supply chain risk and compliance
Managing and adapting to global supply chain risk in a changing world
Meet the experts helping teams navigate medical device compliance
Source Intelligence leaders and industry advisors break down what’s driving complexity through 2026, and what teams can do now to reduce disruption risk, accelerate answers, and improve decision-making across the business.
Turn supplier compliance chaos into clear, defensible decisions
Learn how procurement and risk leaders can align on shared material and supplier data, identify risks, and make faster, defensible decisions across complex bills of material.