Celebrating the Two-Year Milestone and Planning for the Future of Voluntary Genomic Data Submissions

Venue: Online

Location: Online, Pennsylvania, United States

Event Date/Time: Sep 28, 2006 End Date/Time: Sep 28, 2006
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Description

DIA Webinar offer the power and punch of in-person events—all from the convenience of your home or office. This 90-minute, introductory webinar will outline the benefits of a finalized Best Practices Document for the Submission of Data in a Voluntary Genomics Data Submission (VGDS)—the perfect appetizer for DIA’s upcoming two-day workshop, “Best Practices and Development of Standards for the Submission of genomic Data to the FDA.”
Webinar Highlights:
Panel discussion and Q&A with FDA representatives.
Spirited discussion of the VGDS experience.

FEATURED TOPICS:
• Scientific accomplishments showcased in Voluntary Genomic Data Submissions (VGDS) over the past two years.
• Consensus from Q&A sessions about the added value of genomic data in regulatory review.
• New applications associated with VGDS, including other omic platforms and estimates for the impact of pharmacogenomic information in clinical trials.
• Role of VGDS in the Biomarker Qualification Pilot Process.
• Best Practices and Development of Standards in the Submission of Genomic Data to the FDA.

Venue

Online
Online
Online
Pennsylvania
United States
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