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DIA/FDA Biostatistics Industry and Regulator Forum

This event is now offered in a new entirely virtual format.

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Continuing Education Credits

Claiming CE for this event? You must complete a Verification of Attendance Form and email to NAEvents@DIAglobal.org by June 5, 2020.

Access My Transcripts to claim your credit. Available on June 12, 2020.

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Virtual Conference Now Available!

Sessions will be held in ET

Live and On Demand Content is Available to Registered Attendees

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Day 1 May 27, 2020

10:55 AM — 12:30 PM Welcome Remarks and Session 1: Challenges with Global Development and Satisfying Regulatory Requirements

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12:30 PM — 1:30 PM Break
1:30 PM — 3:00 PM Session 2: Statistical, Regulatory, and Operational Considerations for the Use of Digital Health Technologies and Endpoints in Clinical Trials

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3:00 PM — 3:30 PM Break
3:30 PM — 5:00 PM Session 3: Technology Advances for Design and Analysis of Complex Innovative Designs Issues

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Day 2 May 28, 2020

8:30 AM — 10:00 AM Session 4: The Evolution of MID3 and the Intersection of Biostatistics and Clinical Pharmacology in MID3 Clinical Trials

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10:00 AM — 10:30 AM Break
10:30 AM — 12:00 PM Session 5: The Role of Pragmatic Trials for Regulatory Problems

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12:00 PM — 1:00 PM Break
1:00 PM — 2:30 PM Session 6: Safety and Benefit-Risk Assessment

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Day 3 May 29, 2020

9:30 AM — 11:00 AM Session 7: A Community of Networks, Creating, and Leveraging a Network of Distributed Data Supporting Medical Product Development

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11:00 AM — 12:00 PM Break
12:00 PM — 1:30 PM Session 8: Senior Leaders Town Hall Session

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1:30 PM — 2:00 PM Break
2:00 PM — 3:30 PM Session 9: Therapeutic Area Focused Session: Diabetes with a Focus on NASH

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