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Hilton London Docklands Riverside Hotel

Sep 19, 2018 8:00 AM - Sep 20, 2018 5:00 PM

265 Rotherhithe Street , London, SE16 5HW, United Kingdom

Global Clinical Trials Transparency Conference

Session 5: Summary Protocol and Results Information: ClinicalTrials.gov & EudraCT

Session Chair(s)

Matthias  Zerm, PhD

Matthias Zerm, PhD

Lead Expert, Clinical Trial Disclosure and R&D Processes

Merz Therapeutics GmbH, Germany

Are you prepared to posting results in both registries? How do you ensure consistency across registries considering differences in data fields, process (quality review versus purely automated validation) and timing? This session will address procedural aspects, will give insights around the quality control review at ClinicalTrials.gov and provide an outlook on how information contained in clinical trial registries may become more aligned and more meaningful for patients.

Speaker(s)

Thomas  Wicks, MBA

Managing Submissions to Global Registries

Thomas Wicks, MBA

Citeline, United States

Head of Transparency Operations

Heather  Dobbins, PhD

Results Submission “Success”: An Update

Heather Dobbins, PhD

National Institutes of Health (NIH), United States

ClinicalTrials.gov Lead Results Analyst, NCBI/NLM

Smita  Shukla

Improving GSK’s first time acceptance record for Results submissions on ClinicalTrials.gov

Smita Shukla

GSK, United States

Director Clinical Disclosure Reporting

Munther  Baara, MS

Transcelerate Initiative to Improve Data Quality in Clinical Trial Registries

Munther Baara, MS

EDETEK, Inc. , United States

Vice President, Product Strategy and Innovation

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