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Global Pharmaceutical Regulatory Affairs Summit Digital Week
31 May, 2023
1-Day Digital Event
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Day 1

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Day 1
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14:00 - 15:00
Industry FAQs on IDMP Implementation
15:00 - 16:00
The Digital Future: The Impact of Technology on the Future of Regulatory Content Management
16:00 - 17:00
State of the Industry and IDMP

10am EST / 3pm GMT / 4pm CET

  • Gain an Overview of Bristol-Myers Squibb’s Implementation of IDMP
  • Highlight the Opportunities Brought by IDMP and the Importance for Companies to
  • Rise to Meet them, in the Regional Interest and in the eventual Global Landscape
  • Insight into if DADI and SPOR Updates are Resulting in Improved Compliance and Obtaining the Expected Benefits
  • Uncover Industry Thoughts on How Health Authorities Would Benefit from IDMP
  • Jen Klesh - Regulatory Capability Strategist, Manager Global Regulatory Business Capabilities, Bristol-Myers Squibb, USA
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