DIA 2017 Annual Meeting has ended

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DIA 2017 Annual Meeting

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Catherine Craig

8:30am CDT

#21: Successful Drug Development: Best Practices for Drug Development Planning, Agency Interactions, and Regulatory Document Writing S401bc

11:00am CDT

#107: Leveraging Wearables and Sensors in Clinical Trials and mHealth S501abc #117: Postmarketing Safety Studies: Approaches and Regulatory Insights S401a

12:30pm CDT

#132: QuintilesIMS Innovation Theater: The Next Generation of Clinical Development is Here Theater #2

1:15pm CDT

#136: Covance Innovation Theater: Lessons Learned From Deploying Clinical Data Review: Ensuring Patient Safety, Increasing Operational Efficiency and Creating New Insights Theater #2 #137: The Worst Coworker on the Block: Can YOU Work with Difficult People? Yes, You Can! Exhibit Hall

3:00pm CDT

#142: Opening Remarks and Keynote Address Arie Crown Theater

8:00am CDT

#202: People Will Talk: Gathering Insights from Digital Listening S100c

10:30am CDT

#209: Evolving Data Standards and Regulations N228 #211: Sharing the Burden N426b #218: ClinicalTrials.gov: Complying with Requirements in the Final Rule (42 CFR Part 11) and Impacts of 21st Century Cures Act S404bc #219: Safety Evaluation: Transforming Information into Evidence S401a

10:45am CDT

#232: Healthy CRO/Sponsor Relations: “Sole” Mate or Flavor of the Month Exhibit Hall

2:00pm CDT

#240: Mobile Health: Participatory Research N426c #242: Big Data: Current and Emerging Technologies N227b #244: New Trial Design Approaches: Including New Endpoints S501abc #258: Patient-Reported Outcomes (PROs): Hot Topics - Part 1 of 2 S404d

4:00pm CDT

#268: FDA Session: Health IT at FDA N227b #292: How eSource Solutions are Impacting Clinical Research Sites, Patients, Regulators and Drug and Device Companies S400 Concourse #271: Next Generation Patient Recruitment: Part 1 of 2 S501abc #274: Effective Collaboration Between Sponsors and Medical Writing Vendors S403ab #282: Challenges and Issues in Early-Phase Oncology Trials S504abc

8:00am CDT

#302: Does Diversity Matter in Clinical Trials? S100c

10:30am CDT

#308: Quantified Self Tracking N227b #319: A New Age for Physician and Patient Labeling: Recommendations for Innovative Change in How We Communicate S404d

2:00pm CDT

#338: Risk-Based Monitoring: Convergence of Technology, Processes, and People N226 #341: EMA Policy 0070: A Game Changer for Industry N227b #342: Adoption and Implementation of Digital Platforms to Further Patient Interactions N426c #345: Global Perspective on ICH: Part 1 of 2 N228 #346: Understanding the New Common Rule and Its Impact to Industry N426b

4:00pm CDT

#377: Increasing Participation in Clinical Trials Among Under-Represented Populations S505ab #381: Maximizing Success in Partner Collaborations N426b

9:00am CDT

#401: FDA Forum S105

10:45am CDT

#409: Trial Master File: MHRA/EMA Inspections and Sponsor Audit Learnings S402ab #411: Evolving Clinical Trial Guidance and Regulations: Am I Ready? S405b