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Consider the historical path of the Unique Device Identifier (UDI) currently hovering at its real-time usage and the resulting in cost savings and patient safety improvements. Dick Perrin of AHRMM’s Learning UDI Community (LUC) discusses the atomization and use of the same UDI across the continuum allowing for quick identification of recalled products and the patients they may have affected, as well as the potential update of the device or modification of care instructions. Speaker: Dick Perrin, CEO, Active Innovations
Listen as Vicky Lyle, Vice President, Industry Association, Owens & Minor, discusses reducing recall communication difficulties through UDI use and standards development.   This podcast is also available as a webcast.      
Cybersecurity vulnerabilities and intrusions pose risks for every hospital and its reputation. Become aware of what you can do to prevent cyber security in your facility.
AHRMM Podcast on how supply chain should be interdepartmentally conversing to determine the handling of human-origin medical products and their UDIs.
A short introduction to the CMS Meaningful Use 3 Rule and how implementing UDI within the healthcare setting and moving toward the full GS1 will reduce costs and improve inventory management while providing accurate data reporting and complete patient EHR information. Ultimately, these changes will lead to knowledge-based decision making and improved quality of patient care.
As UDI capture and exchange becomes more prevalent across the healthcare ecosystem and as implantable device information is linked to patient outcomes there are a number of expected benefits to look at. Find out how UDI will improve patients safety and supply chain purchasing for years to come.
Get the basics on what healthcare supply chain and manufacturers, together with clinical and IT departments, must do to implement the Unique Device Identifier and adverse event reporting, and the subsequent effects that will trickle-down to individual patients and the global health population.
Hear one provider’s ongoing process of UDI implementation, from deciphering acronyms and educating interdepartmental staff, to working with vendors to redesign ERP software to meet FDA data capture and reporting regulations, all while creating procedures for others to follow.