6th Edition Regulatory Information Management and Data Quality for Pharma Sector 2019

  • Apr 2019
  • Germany

Description

Topics
  • Manage effective compliance work and IDMP strategy despite missing EMA guidelines
  • Benchmark with practitioners ahead of the curve
  • Focusing on the 1st iteration in practice
  • Preparing for 2nd and further iterations
  • XEVMPD to IDMP: Data migration questions
Who should Attend

Senior attendees from life science industy involved in:

  • Regulatory Affairs
  • Regulatory Affairs Operations
  • Document Management
  • Submissions
  • Central IS/IT Teams
  • Regulatory IS/IT
  • Regulatory Information
  • Regulatory Systems
  • Pharmacovigilance
  • Documentation & Information Services
  • Data Governance
  • Master Data Management
  • Product Information Management Domain
  • Data Quality

Past Events

Important

Please, check "Edition Regulatory Information Management and Data Quality for Pharma Sector" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Pharma
Science: Life Sciences & Biology
Technology: Biotechnology, Data management

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