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Hyatt Regency Bethesda

2015 年 09 月 17 日 7:30 上午 - 2015 年 09 月 18 日 3:15 下午

One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814-5326

Clinical Trial Disclosure & Data Transparency

Explore the impact of current and pending federal regulations on data transparency from industry, clinical, and regulatory perspectives’.

Session Chair(s)

Robert  Paarlberg, MS

Robert Paarlberg, MS

Principal

Paarlberg & Associates LLC, United States

Speaker(s)

Nicholas C. Ide, MS

Updates to the ClinicalTrials.gov Protocol Registration and Results System (PRS)

Nicholas C. Ide, MS

National Institutes of Health (NIH), United States

Chief Architect, ClinicalTrials.gov, National Library of Medicine

Rebecca  Williams, PHARMD, MPH

Updates to the ClinicalTrials.gov Protocol Registration and Results System (PRS)

Rebecca Williams, PHARMD, MPH

Essex, part of Emmes Group, United States

Senior Clinical Trials Subject Matter Expert

Noemie  Manent, PHARMD

Updates to the EudraCT Database

Noemie Manent, PHARMD

European Medicines Agency, Netherlands

TDA-CTT Change Management Lead

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