Integrated Data Management Platform
The European Medicines Agency (EMA) is gearing up towards the implementation of the ISO Identification of Medicinal Products (IDMP) with a target deadline for full implementation in 2018 for medicinal products.
IDMP poses several challenges to the pharmaceutical industry, the key being the ability to integrate disparate data from multiple systems managed by multiple functional areas within an organization. While being a technology and an integration challenge, IDMP also poses organizational and political challenges given that it requires the collaboration and cooperation among many functional units, which have been traditionally independent and siloed for a long time.
Most importantly, most of the information is embedded in documents such as Summary of Product Characteristics (SmPCs), CMC documents, cover letters, electronic application forms, etc. Extracting data from documents is going to be a major challenge.
Our ReALM® IDMP Solution:
We have extended our ReALM® platform to support IDMP requirements for Iteration 1.
We would be glad to arrange for a demo. Please send us a request to firstname.lastname@example.org.