DIA Annual Meeting 2014

June 15, 2014 – June 19, 2014
San Diego, CA (USA)

Sunday, June 15, 8:30 AM - 12:00 PM

Japan's Regulatory Environment:  Overview of the Organization, Processes, Systems and Changes Affecting Pharmaceutical Development
Alberto Grignolo, Corporate Vice President, Global Strategy and Services

Sunday, June 15, 1:00 PM - 4:30 PM

Tutorial: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges and Decision Criteria
Paul Bridges, Corporate Vice President, Worldwide Head, Consulting
Katie Connelly, Vice President, Strategic Resourcing and Operations

Monday, June 16, 11:00 AM - 12:30 PM

R&D and Technology Outsourcing Today:  An Industry Update
Chair: Keith Wenzel, Senior Director, Global Alliances

Tuesday, June 17, 8:00 AM - 9:30 AM

Regulatory and GCP Quality Trends in Emerging Markets
Deborah Wade, Vice President, Process Quality Management

Clinical Outcomes Assessments/Patient Engagement Symposium
Chair: Keith Wenzel, Senior Director, Global Alliances

Tuesday, June 17, 10:30 AM - 12:00 PM

Drug Development with Reimbursement in Mind:  Obtaining the Input of Payers to Inform Clinical Trial Design
Chuck Stevens, Vice President, Reimbursement and Market Access

Tuesday, June 17, 1:30 PM - 2:30 PM

Electronic Tools for Trial Material Supplies Management:  Closing the Gaps to Ensure Full Control, Traceability and Visibility
Andrey Gurachevsky, Senior Technical Logistics Coordinator

Tuesday, June 17,  3:30 PM - 5:00 PM

How CROs Can Better Support Sponsor Protocol Development
Jeffery Fairbairn, Senior Director, Partnerships

Wednesday, June 18, 8:00 AM - 9:30 AM

Clinical Trials Technology Implementation:  Bringing Together Patient-and Site-centric Approaches
Chair & Presenter: Bill Byrom, Senior Director, Product Strategy

CDISC BRIDG Implementation:  A Model for System Interoperability and as a Data Base Model
Terry Hardin, Director, Clinical Data Standards

Wednesday, June 18, 3:30 PM - 5:00 PM

Using Technology and Processes to Effectively Manage Regulatory Documentation Requirements for Global Late Phase Clinical Research
Kate Trainor, Vice President, Late Phase, Global Head Project Management & Technology

Project Management Plays Critical Roles in the New Challenging Environment
Alberto Grignolo, Corporate Vice President, Global Strategy and Services

End-to-End Data and Metadata in Today's Clinical Trials
Chair: Keith Wenzel, Senior Director, Global Alliances

The Role of Orphan Drug Legislation in Emerging Markets
Vann Parker, Principal Consultant

Visit PAREXEL at Booth #1823 in the exhibit hall.

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