DIA 2020 Virtual Global Annual Meeting has ended

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DIA 2020 Virtual Global Annual Meeting

11:00am EDT

#106 SL: Clinical Trials in a Digital Age: A Modern Approach to an Outdated Model TBD

1:30pm EDT

#119 L: How Do You Oversee and Manage New Centralized/Remote/Site Monitoring Models? What Should you Measure to Gain Insights? TBD

3:30pm EDT

#129 SL: The Rare Disease Clinical Outcome Assessment Consortium: Aiming to Fulfill Unmet Drug Development Endpoint Measurement Needs TBD #131 L: Engaging Patients to Support the Modernization of ClinicalTrials.gov TBD

9:30am EDT

#210 SL: Clinical Electronic Structured Harmonized Protocol (CeSHarP): ICH M11 - Status Update TBD

11:30am EDT

#221 L: Non-Traditional Clinical Trials Require a Non-Traditional Workforce TBD #224 SL: Sponsor and Regulator Challenges, Risks, and Mitigation Strategies for Ensuring Third-Party Oversight of Vendors: Is Your Study Data at Risk? TBD

3:15pm EDT

#242 L-RT: Round Table Discussion: Examining Diversity in Clinical Trials TBD

2:00pm EDT

#332 SL: Optimizing Communication with Patients to Support Meaningful Feedback into the Research Process TBD

4:00pm EDT

#339 SL: The Development of Novel Digital Endpoints TBD

8:00am EDT

#402 L: FDA Perspectives on Modernization of Clinical Trials: Real World Evidence, Decentralized Clinical Trials, and Digital Health Technologies TBD

9:30am EDT

#411 L: Qualification and Oversight in Decentralized Trials: Practical Considerations for Clinical Operations and Quality Oversight TBD

11:30am EDT

#422 L: How the FDA’s MyStudies Platform is Accelerating the Use of Digital Technology in Clinical Research and Clinical Trials TBD

5:00pm EDT

#505 OD: ON DEMAND - Older People Can’t Use ePRO and Other Industry Myths: An Interactive Debate TBD #507 OD: ON DEMAND - Managing Global Clinical Trials in Emerging Regions: Latin America TBD #509 OD: ON DEMAND - Faster, Better, Cheaper: The Changing Role of Real World Data in Drug Development TBD #549 OD: ON DEMAND - Translating Frequently Collected Patient Experience Data into Meaningful Trial Endpoints TBD