IDMP Compliance Challenge and Regulatory Information Management 2015

  • 17-19 Jun 2015
  • London, United Kingdom

Description

Topics
  • 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
Who should Attend

Attendees from pharmaceutical companies.

Past Events

Important

Please, check "IDMP Compliance Challenge and Regulatory Information Management" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Pharma
Technology: Data management

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