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

Jen Klesh
Regulatory Capability Strategist, Manager Global Regulatory Business Capabilities at Bristol-Myers Squibb, USA
Speaker

Profile

Jen has worked in regulatory for over 18 years spanning IDMP preparation, xEVMPD implementation, global eCTD onboarding, dossier publishing, and document publishing. In her current role, Jen serves as the business lead for BMS’ IDMP Solution Selection project and Data Readiness. She is also the BMS representative on the EFPIA eCTD Working Group. Jen holds a BA in Visual Communications (an interdisciplinary degree combining Computer Science, Media Analysis, and Graphics Design) and an MBA with a specialty in Leadership.

Agenda Sessions

  • State of the Industry and IDMP

    16:00