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Monday, June 25
 

11:00am

#117: Beyond Robotics Process Automation: Next Generation Integrated QMS for R&D Room 205C

3:00pm

#154: Bayesian Application in Small-Sized Clinical Trials Room 256
 
Tuesday, June 26
 

8:00am

#215: Pediatric and Rare Disease Drug Development Room 256 #217: Triple-A RWE: Adequate Data, Appropriate Study Designs, and Actionable Evidence Room 210AB

10:30am

#226: Regulators’ Utilization of Real-World Data in Pharmacovigilance Activities Room 253AB

2:00pm

#251: Risk Management: New Directions Room 253AB

2:15pm

#269B: Avoiding Rejection on your "First Date" with EMA Policy 0070 E and E Exhibit Hall

4:15pm

#294: Sustainable Healthcare Funding Room 258AB #276: Patient Engagement in Pharmacovigilance Room 253AB #290: Priority Review Vouchers: Here to Stay and Worth the Effort? Room 206AB
 
Wednesday, June 27
 

8:00am

#315: Can I Implement That Now? Efficiently Managing Post-Approval CMC Changes Room 208

10:30am

#329: Reducing the Burden of Drug Safety Risk Minimization Programs on the Healthcare System: How Do We Do So and What Has Been Learned to Date? Room 253AB #338: You've Got Data #now what? Room 157AB #345: Unmet Medical Need: Path Forward – Creating a Commonly Agreed Criteria Globally Room 252AB

4:00pm

#385: Does Sourcing Strategy Matter? Executives Debate the Influence of Outsourcing Model on Clinical Trial Execution Room 258C
 
Thursday, June 28
 

9:00am

#406: Improving Efficiency and Effectiveness in Data Management of Pediatric, Rare Disease, and Oncology Trials Room 205C