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Medidata Solutions: Optimizing Clinical Trials: Concept to Conclusion^®
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Tufts, BI, INC and Lundbeck are heading back to the classroom »

Grab your school bags and join them for an enlightening morning of discussion with leading industry experts on the impact of study design on execution, cost, speed and data quality. This free seminar will discuss strategies for better trial design and execution; maximizing on operational, financial and patient opportunities; and reducing time and cost from concept to conclusion of clinical trials.

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Our panel of speakers will:

Address advances in protocol design and development, study planning and budgeting, study execution and delivery, and reporting;

Challenge the efficiency of some activities (e.g. protocol/study design) and debate the very need for others (e.g. targeted source document verification, serious adverse event reconciliation);

Use real case studies to illustrate conclusions; and

Demonstrate how delivering upon this strategy has been paramount to the success of current and future clinical trials.

Seminar Details

Who Should Attend: Senior Management and Executives, Clinical Operations and Budgeting Professionals, Project/Program Managers, Medical Writers

*Please note that all parking expenses will be complimentary of Medidata.

Date: Tuesday, 24 September, 2013	Time: 08:30-14:00 CET
Location: Frankfurt Marriott Hotel Hamburger Allee 2 60486 Frankfurt am Main Germany Map

Featured Speakers:

Optimizing Trial Design
Stella Stergiopoulos
Project Manager
Tufts Center for the Study of Drug Development

Structured Protocols beyond Bench-Marking
Miguel Perez-Vazquez
Program Manager
Boehringer Ingelheim

Clinical Challenges in Study Start-Up & Execution
Sally Osmond
EVP & General Manager Cardiovascular & Endocrinology
INC Research

Data Challenges Across the Clinical Trial Lifecycle
Alastair Clewlow
Head of Data Management
Lundbeck

From Concept to Conclusion: Advancing the Entire eClinical Landscape
Richard Young
Director
Medidata Solutions

*If you are unable to attend but interested in this topic, please contact Rachel Lowrey at rlowrey@mdsol.com.

Optimizing Clinical Trials: Concept to Conclusion™