About the webinar

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.

Join Source Intelligence’s regulatory and supply chain experts for a focused, medical-device-specific session on where chemical and supply chain compliance breaks down, and what leading manufacturers are doing to get ahead of it. This webinar cuts through theory to show how to operationalize compliance across devices, materials, and suppliers without slowing sourcing or innovation.