DIA 2017 Annual Meeting has ended

Create Your Own Event

DIA 2017 Annual Meeting

EC

Emma Coppin

7:00am CDT

Attendee, Speaker, and Exhibitor Registration TBA

7:30am CDT

Coffee and Light Refreshments TBA

8:30am CDT

#102: The Evolution of Evidence Generation: Real-World Evidence and the Next Generation of Decision Making S100a

10:00am CDT

Exhibit Hall Open TBA

11:00am CDT

#109: Submission Dossiers: Communications Excellence to Drive Speed and Quality S503ab

12:00pm CDT

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

2:00pm CDT

#140: SAS Institute Inc. Innovation Theater: Clinical Analytics Workflow Optimization Theater #2

3:00pm CDT

#142: Opening Remarks and Keynote Address Arie Crown Theater

4:30pm CDT

Opening Reception TBA

5:30pm CDT

#147: Appian Innovation Theater: Product Lifecycle Management In The Digital Era Theater #2

7:00am CDT

Attendee, Speaker, and Exhibitor Registration TBA Coffee and Light Refreshments TBA

8:00am CDT

#201: Paying for Value in Biopharmaceuticals: Trends in the United States S105

9:45am CDT

#207: Veeva Systems, Inc. Innovation Theater: 2017 Unified Clinical Operations Survey Theater #1

10:30am CDT

#218: ClinicalTrials.gov: Complying with Requirements in the Final Rule (42 CFR Part 11) and Impacts of 21st Century Cures Act S404bc

11:30am CDT

1:00pm CDT

#238: Veeva Systems, Inc. Innovation Theater: Tomorrow's Clinical Trial, Powered by Modern EDC Theater #1

2:00pm CDT

#256: Post-Trial Access: Ensuring Patient Access Across the Development Spectrum N230b

3:00pm CDT

Refreshment Break TBA

3:25pm CDT

#267: Veeva Systems, Inc. Innovation Theater: Unified RIM: End-to-end Submissions Development—from Planning Through Archival Theater #1

7:00am CDT

Attendee, Speaker, and Exhibitor Registration TBA Coffee and Light Refreshments TBA

8:00am CDT

#303: International Regulatory Convergence S100a

9:30am CDT

Coffee Break TBA Exhibit Hall Opens TBA

10:30am CDT

#320: The Brave New World: The Ongoing Globalization of Pharmacovigilance N226

11:30am CDT

2:00pm CDT

#344: Minding the Gaps: Using Totality of Evidence in the Clinical and CMC Contexts to Support Regulatory Approval S404a

3:00pm CDT

Refreshment Break TBA

4:00pm CDT

#364: Risk-Based Monitoring: Convergence of Technology, Processes, and People: Panel Discussion N226

8:00am CDT

Attendee and Speaker Registration TBA Coffee and Light Refreshments TBA

9:00am CDT

#401: FDA Forum S105

10:30am CDT

Coffee Break TBA

10:45am CDT

#410: Of Course My Data Has Integrity … And I Can Prove It S405a