The 12th Conference in Data Series: IDMP Compliance Challenge: Progressing on Master Data and Systems Harmonisation 2015 provides an insight on the impact of ISO IDMP and key preparatory activities for ISO IDMP pharmacovigilance legislation before it takes effect in 2016. Topics include:
- How to prepare IDMP compliance by figuring out data at hand and how to draw together data you do not have
- How to manage RIM lifecycle of pharmaceutical products across multiple silo systems with very limited interoperability
- Learning from master data management projects supporting IDMP compliance and data harmonisation across the group whilst building a well-integrated Regulatory Information Management system
- How to draw and maintain information about packaged medicinal products to prepare for IDMP compliance and how to work towards a single, authoritative data repository
Who should Attend
Attendees from pharmaceutical companies.
