To help facilitate compliance to the new submission standard Extended EudraVigilance Medicinal Product Dictionary (XEVMPD), NNIT and partner Mission3 offer Global Track GxPD. The solution allows life science businesses to immediately start collecting the required XEVMPD data from internal systems and submit in the proper format.As of 2 July 2012 life science businesses have to adhere to EMA’s XEVMPD standard. To many companies this poses a genuine challenge as the entire process of data capture and submission process is subject to change. We can help you comply on time.
Comprehensive XEVMPD Data ManagementTake advantage from a web-based and highly user friendly solution integrated with Microsoft SharePoint:
The solution can be extended to your entire Regulatory Information Management system, including regulatory planning and tracking, as well as manage and track health authority correspondence.Call us today and let’s have an informal and preliminary talk about how NNIT can help you turn XEVMPD requirements into business advantage.
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