Agendas
8:30 AM — 12:00 PM
Tutorial #1 – IDMP? What Is That and How Do I Get Started?1:00 PM — 1:30 PM
Welcome and Opening Remarks1:30 PM — 3:00 PM
Plenary Session 1: FDA Update3:00 PM — 3:30 PM
3:30 PM — 5:00 PM
Plenary Session 2: Other Regions Updates5:00 PM — 6:30 PM
7:30 AM — 8:30 AM
8:30 AM — 10:00 AM
Session 1 Track 2: Preparing for the New Module 1 (3.3 Format)8:30 AM — 10:00 AM
Session 1 Track 3: eTMF & eSignatures: Issued, Applied, Inspected8:30 AM — 10:00 AM
Session 1 Track 4: RIM in the Cloud - Benefits and Challenges10:00 AM — 10:30 AM
10:30 AM — 12:00 PM
Session 2 Track 1: Organizational Implications to the Changing RIM Environment10:30 AM — 12:00 PM
Session 2 Track 4: Master Data Management, IDMP and RIM – How Can They Relate?12:00 PM — 1:30 PM
1:30 PM — 3:00 PM
Session 3 Track 3: How Audit and Inspection Ready is Your Organization?1:30 PM — 3:00 PM
Session 3 Track 4: IDMP Implementation - Opportunities and Challenges3:00 PM — 3:30 PM
3:30 PM — 5:00 PM
Session 4 Track 4: IDMP Session 27:30 AM — 8:30 AM
8:30 AM — 10:00 AM
Session 5 Track 4: IDMP Implementation - Where is the Correct Data?10:00 AM — 10:30 AM
10:30 AM — 12:00 PM
Session 6 Track 1: Regulatory Operations Outsourcing - Recipe for Success10:30 AM — 12:00 PM
Session 6 Track 4: Mergers and Acquisitions: Implications for RIM12:00 PM — 1:30 PM
1:30 PM — 3:00 PM
Session 7 Track 1: Ask The Experts Session1:30 PM — 3:00 PM
Session 7 Track 2: Ask The Experts Session1:30 PM — 3:00 PM
Session 7 Track 3: Ask The Experts Session1:30 PM — 3:00 PM
Session 7 Track 4: Ask The Experts Session3:00 PM — 3:15 PM
3:15 PM — 4:45 PM
Closing Plenary: "Ask The Regulators" Session4:45 PM — 5:00 PM
Closing Remarks