Agendas

The DIA Annual Meeting, the largest multidisciplinary event that brings together a global network of life sciences professionals to foster innovation that will lead to the development of safe and effective medical products and therapies to patients.

Day 1 Jun 15, 2015

8:30 AM — 10:00 AM

How Pharmaceutical Companies and CROs Are Harnessing Big Data and Cloud Computing to Increase R&D Innovation, Efficiency, and Collaboration

8:30 AM — 10:00 AM

How Sponsors Are Solving the Unique Data Collection Challenges of Late-Stage Studies

11:00 AM — 12:00 PM

Evolving Your Regulatory Information Management Strategy to Meet the Changing Business Environment

11:00 AM — 12:00 PM

Integrating Patient Engagement with EHR Data and eSource for Better Studies

Day 2 Jun 16, 2015

8:00 AM — 9:30 AM

Implementing Risk-Based Monitoring

8:00 AM — 9:30 AM

International Organization for Standardization (ISO) Identification of Medicinal Products (IDMP): Will Your Company Be Ready by 2016?

10:30 AM — 12:00 PM

FDA Study Data Technical Conformance Guide (Part 1 of 2): An Overview

10:30 AM — 12:00 PM

How to Trust Data from Wearable Devices Used in Clinical Trials

1:30 PM — 2:30 PM

Developing Online Communities: Perspectives for Site and Patient Engagement

1:30 PM — 3:00 PM

FDA Study Data Technical Conformance Guide (Part 2 of 2): An Interactive Q&A Session

3:30 PM — 5:00 PM

Data and Evaluation Needed for Robust Evidence: Regulators' Challenges

3:30 PM — 5:00 PM

How Risk-Based Monitoring and eSource Methodologies Are Impacting Clinical Sites, Patients, Regulators and Sponsors

Day 3 Jun 17, 2015

8:00 AM — 9:00 AM

CDISC SHARE Repository: Laying the Tracks and Building the Stations for This New Metadata Train

8:00 AM — 9:30 AM

Mapping the Future for Trial Master File: Advancing Standards by Harmonizing Clinical and Technical Strengths

10:30 AM — 12:00 PM

Digitization of Clinical Trials: Check the Pulse on Bringing Benefits to Patients

10:30 AM — 12:00 PM

Electronic Standardized Data in Regulatory Submissions

1:30 PM — 3:00 PM

Frontier Issues in Electronic Information Integrity Today

1:30 PM — 3:00 PM

Searching for the Gold Nuggets: Text Analysis in Clinical Data

3:30 PM — 5:00 PM

CFAST Initiative: Potential to Dramatically Increase ROI and Reduce Timelines in the Conduct of Clinical Trials

3:30 PM — 4:30 PM

The Critical Role of Document Management Supporting Submissions: Regulatory Operations, IT and Vendor Perspectives

Day 4 Jun 18, 2015

9:00 AM — 10:30 AM

Bring Your Own Device (BYOD) Approaches to the Collection of Electronic Patient-Reported Outcome Data in Clinical Trials

9:00 AM — 10:30 AM

Tired of Reinvesting in Old R&D Systems? Several Large Pharmaceutical Companies and Other Leaders Are Flipping Paradigms

10:45 AM — 12:15 PM

mHealth / mClinical and Clinical Trials: A Candid Discussion on Opportunities and Risks

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DIA 2015 51st Annual Meeting: Develop. Innovate. Advance.

Agendas

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