IDMP Compliance Challenge and Regulatory Information Management 2015 covers topics such as:
- RIM lifecycle of pharmaceutical products across multiple silo systems with very limited interoperability
- The impact of ISO IDMP and organise subsequent prioritization of key preparatory activities
- Information about packaged medicinal products to prepare for IDMP compliance
- IDMP compliance: Figuring out data at hand and how to draw together data they do not have
- Master data management projects supporting IDMP compliance and data harmonisation across the group
IDMP Compliance Challenge and Regulatory Information Management 2015 brings together attendees from pharmaceutical companies.
