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Regulatory Submissions, Information, and Document Management Forum

Agenda

Day 1 Feb 06, 2018

11:00 AM — 12:15 PM Session 6 Track 2: The Increasingly Critical Roles of RIM Systems and Their Expanding Number of Use Cases Beyond Regulatory Affairs
1:45 PM — 3:00 PM Session 7 Track 2: How to Compete in the Data-Driven Digital Transformation in the Pharmaceutical Industry?
3:30 PM — 4:45 PM Session 8 Track 2: Transforming Regulatory Information Management Through Innovation

Day 2 Feb 07, 2018

8:30 AM — 9:45 AM Session 9 Track 2: Driving Innovation in Regulatory Technology within Life Sciences
10:15 AM — 11:30 AM Session 10 Track 2: Artificial Intelligence (AI): The Next Frontier

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On-Demand Webinars

EDM and ERS - Hot Topics and Tools of the Trade

Enterprise Ontology Approach to System Implementation and Process Development to Minimize Organizational Disruption

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Regulatory Submissions, Information, and Document Management Forum Resource Guide

Preconference Short Courses

Regulatory Content and Submissions Primer: Tracking Content from Conception to Interment

Global Identification of Medicinal Products: Applied Principles and Practical Benefits from Compliance and Beyond

Essentials for Compiling/Publishing Compliant Electronic Submissions (eCTDs)