Agenda


The agenda is subject to change.

Time

Session

MONDAY

08.00 - 09.00 Onsite registration
09.00 - 10.30

Welcome & Keynote Speakers

How PhUSE Collaborations Assist Regulatory Review
– Crystal Allard, FDA

Why Data Sharing from Clinical Trials Really Matters
– Trish Groves, The BMJ

10.30 - 11.00  Morning Break
11.00 - 12.30

 Working Group Breakout Sessions

  • Data Transparency
  • Nonclinical Topics
  • Optimizing the Use of Data Standards
12.30 - 13.30  Lunch
13.30 - 15.00

 Working Group Breakout Sessions

  • Data Transparency
  • Nonclinical Topics
  • Optimizing the Use of Data Standards
15.00 - 15.30  Afternoon Break
15.30 - 17.00

 Working Group Breakout Sessions

  • Data Transparency
  • Nonclinical Topics
  • Optimizing the Use of Data Standards
17.00 - 20.00

Networking Session
– Light refreshments provided

TUESDAY

09.00 - 10.30

Working Group Breakout Sessions

  • Data Transparency
  • Nonclinical Topics
  • Optimizing the Use of Data Standards
10.30 - 11.00 Morning Break
11.00 - 12.30

Working Group Breakout Sessions

  • Data Transparency
  • Nonclinical Topics
  • Optimizing the Use of Data Standards
12.30 - 13.30 Lunch
13.30 - 14.30 Panel Discussion:
Navigating Regulatory Guidance – Separating Fact From Fiction  
– Regulatory & Industry Panelist
14.30 - 15.00 Wrap-Up & Closing Remarks
15.30 Conference Close

 

 

 

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