Teaming to deploy best-in-class solution for rapid UDI compliance
The FDA UDI (Unique Device Identifier) mandate was initiated to enable better traceability of medical devices throughout the supply chain and to improve the information available for managing product quality issues that could potentially impact the patient. Other global Health Authorities such as the Global Harmonization Task Force (GHTF) are also enacting similar requirements with which multinational companies will soon have to comply.
Inspirage/Oracle/USDM 5-Step UDI Solution Our USDM and Oracle have partnered to deliver a best-in-class proven rapid start UDI solution, enabling Medical Device customers to meet the imposed sunrise date. The Inspirage solution combined with USDM’s expertise in UDI and FDA compliance offers customers with a proven way to help meet UDI regulations.
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