Register today to attend the Global Regulatory Affairs 1 Day Digital Event. Free-to-attend, this event brings you an overview of IDMP implementation with regards to current trends and timelines as well as insight into the latest digital strategies that will lead you towards digital transformation. To find out more about future sponsorship opportunities, please contact partners@informaconnectls.com.
31 May 2023
Industry FAQs on IDMP Implementation
9am EST / 2pm BST / 3pm CEST
Asphalion’s experience with the Industry most asked questions related to the IDMP implementation and how the perception of Industry on IDMP is driving their activities to be compliant.
Answers on IDMP timelines including IDMP implementation current status and the impact of the web-based eAF
Overview of the trends on activities to prepare for IDMP
Speaker:
Lidia Cánovas Key Accounts Director
Asphalion
Beatriz Ugalde Regulatory Data Manager
Asphalion
Helena Catena Data Project Manager
Asphalion
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The Digital Future: The Impact of Technology on the Future of Regulatory Content Management
10am EST / 3pm BST / 4pm CEST
Insight into the Strategies towards Digital Transformation
Overview of a Regulatory Platform to Harmonize Regulatory content as a Foundation for the Digital Future
The role of automation in enhancing Regulatory Content Management and eSubmissions
Speakers:
Jackie Leslie Category Specialist, Life Sciences
Esko
David Turner Consultant - Publishing Automation, Digital Transformation, and Content Technologies
Data Conversion Laboratory (DCL)
Regina Lynn Preciado Senior Director of Content Strategy Solutions
Content Rules
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The State of the Industry and IDMP Compliance
11am EST / 4pm BST / 5pm CEST
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
Speaker:
Jen Klesh Associate Director, Medicinal Product Data Management
Bristol Myers Squibb
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REGISTER NOW – Please select the webcast(s) you wish to attend and enter your contact details