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Hear Jay Crowley, Senior Advisor for Patient Safety with the FDA Center for Devices and Radiological Health discuss the pending FDA UDI regulations for the U.S. medical device market, and how you, as a medical device manufacturer, can start preparing now.
David Leedam, the Head of eCommerce EMEA, APAC, for Siemens Healthcare Diagnostics, provides an overview of Siemens' successful harmonized approach to standards implementation.
Covers how to achieve reduced supply costs and increased efficiencies through data enrichment, categorization, HCPCS assignment, contract optimization and sourcing new products.
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