DIA 2018 Global Annual Meeting has ended

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DIA 2018 Global Annual Meeting

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8:00am EDT

#303: Regulatory and Ethical Considerations with Placebo Administration Using a Central Venous Access Device in a Pediatric Trial Room 258C #304: Data and Quality Approaches to Informing Global Investigative Site Selection Room 258AB #305: Building a Roadmap to the Implementation of the Risk-Based Monitoring Process: Facilitating the Perspectives of All Stakeholders Room 254AB #308: How Do Patients and Other Multi-Disciplinary Stakeholders Collaborate to Develop Patient Registries which Accelerate Research? Room 151AB #309: Evolution and Harmonization of First-in-Human Guidelines Room 156ABC #316: Opportunities for Efficient and Innovative Study Designs Room 256

10:30am EDT

#337: Balancing Regulatory, Medical, and Operational Pillars to Get Pediatric Trials Done Globally Room 156ABC #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 #330: Artificial Intelligence: Robots Taking Over Clinical Research Room 253C #331: Rebuilding or Building a Research Site in the Year 2020 Room 254AB #332: Clinical Data: Let’s Get to the Source and Streamline it to the End Room 208 #335: Collaboration Across the Medical Affairs Ecosystem to Advance Patient Care Room 257AB

2:00pm EDT

#361: A New Way of Authoring and Reviewing Documents for Clinical Development Room 258C #358: Expedited E2B Safety Reporting in Interventional Clinical Trials: Convergence of Global Expectations? Room 253AB #360: Implementation of eConsent and Other Digital Clinical Trial Innovations Room 258AB #364: Achieving Customer Centricity to Advance Patient Care Through Innovative Communication Channels Room 210C #366: Gene Therapy Clinical Trials: Current Challenges Room 156ABC #375: Statistical Challenges in Assessing Drugs’ Efficacy by Utilizing Biomarker Endpoints Room 256

4:00pm EDT

#384: Innovations in Managing Global Clinical Supplies Room 258AB #385: Does Sourcing Strategy Matter? Executives Debate the Influence of Outsourcing Model on Clinical Trial Execution Room 258C #386: Bring Your Own Device ePRO: Hold the Relish, or No Holds Barred? Room 257AB #390: Special Population Study Challenges Room 156ABC #397: Design and Statistical Considerations for Real World Evidence to Support Regulatory Decision Making Room 256