Solution for Creation and Submission of Extended EudraVigilance Product Report Message (XEVPRM)- eMPDExpert™
European Medicines Agency requires that by July 2, 2012, information on medicinal products for human use authorized or registered in the Union is submitted electronically. XML file referred to as the Extended EudraVigilance Product Report Message (XEVPRM) has to be generated for the submission.
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eMPDExpert™ is part of INFOTEHNA myPharmaExpertTM Suite that facilitates data collection and enables companies to submit their EV Product Report Message easily and on time. |
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eMPDExpert™ features:
- Structuring and collecting XEVPRM data
- Creation of XEVPRM
- Electronic submission
- User-friendly interface
- Drop-down lists
- One-time input of information
- Direct submission
- Re-use of information and documents
Solutions
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