Uppsala Monitoring Centre (UMC) believes that IDMP represents a game-changing development in the world of pharmacovigilance by establishing a common language and facilitating the effective exchange of vital medicinal product data across the entire drug development and regulatory lifecycle. By enabling harmonized data exchange, IDMP enhances our ability to identify, evaluate, and mitigate risks associated with medicinal products. In an open, 1 hour webinar on 14 June 2023, UMC will welcome interested parties to learn more about the current status of IDMP and how various global stakeholders, including UMC, are collaborating to implement the standards and make them a reality.
UPDATE: Recordings of the webinar are now available – see below
A key UNICOM aim is to improve the processing and analysis of individual case safety reports (ICSR) that describe one or more suspected adverse drug reactions (ADRs) that occur in a single patient. To this end, the organisation has released the working paper “IDMP Coding Principles and Guidance for ICSRs“.
The working paper provides recommendations for practical IDMP implementation aspects (for example, PhPID generation) and for handling drug information in general (such as grouping concepts, use of name parts), aimed at improving ICSR data management and pharmacovigilance analysis.