With IDMP Compliance becoming mandatory by 2023, Pharma companies have begun the arduous task of understanding the requirements of IDMP compliance, data analysis and digitizing the data from SmPCs and eCTD Module 3 documents into IDMP compliant data sets to feed into regulatory submission systems. Most of the data is in unstructured regulatory documents and requires to be extracted and tagged appropriately. This involves lot of manual effort and precious time from medical experts to ensure the extracted data is codified properly and validated.
Time-bound regulatory mandate
Unstructured Regulatory Documents
Manual Review Process
Expert intervention
DF IDMP AI helps achieve efficiency and compliance during the IDMP data life cycle. Starting from data extraction using our OCR models, to text mining using our NER models tailored for IDMP data standards, the process of generating a structured data set is automated to a large extent. The medical experts can focus on validating the output through a user-friendly UI. The IDMP data set is then made available to any down stream application such as a regulatory submission system or for analytics and insights.