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 Management
Take advantage from a web-based and highly user friendly solution integrated with Microsoft SharePoint:

• GlobalTrack GxPD allows you to immediately start collecting product data
• User access according to defined roles providing high security
• Manual data entry is minimized
• Data is validated automatically
• Global Track GxPD can automatically aggregate and present data from existing legacy systems as it features out-of-the box integration of e.g. Documentum, FirstDoc, SAP, excel, access, Oracle
• Global Track GxPD lets you manage all current XEVMPD needs and will also support IDMP (Identification of Medicinal Products) submission functionalities when this standard is effective in 2015

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.