Is 2017 an IDMP year at all?


Download Whitepaper

By clicking ‘Submit’ button, you are agreeing to opt-in to communications from ArisGlobal and use of the above information for ArisGlobal products, news & updates.

Note: You can unsubscribe to email communication from ArisGlobal any time.

Despite delays from EMA in their compliance deadline, now is a good time for regulatory affairs to work on recommendations from an IDMP (Identification of Medicinal Products) readiness assessment. And for those that haven’t embarked on the assessment journey yet, it’s high time to understand how technology innovation in regulatory compliance space can launch and support your assessment phase.

This paper looks at how technology can support the move toward IDMP compliance. Learn how leveraging technology can:

  • Boost productivity of your regulatory data team by using automation to quickly convert existing xEVMPD compliant data into a central data hub that is xEVMPD + ISO IDMP compliant
  • Improve data quality by validating a company’s central product data dictionary against relevant current xEVMPD business rules to ensure all required data is in place
  • Create a sustainable maintenance process by making electronic gateway-based submissions to the xEVMPD database in readiness for IDMP
  • Reduce manual eff­ort of IDMP data augmentation to xEVMPD data with technology innovations in natural language program-based unstructured document data extraction