Data Management STREAM
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How Clinical Data Studio Works Across The Organization
6/19/2024
Explore how Clinical Data Studio converts data into actionable knowledge, fostering seamless collaboration across teams to enhance the efficiency and effectiveness of clinical trials.
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psiXchange: Intelligent, Automated Safety Reporting
3/25/2024
Say goodbye to manual burdens and embrace efficiency by fully automating your safety reporting. This will significantly cut down on effort and costs, all while enhancing compliance standards.
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The Importance Of Reliable Data To Clinical Trial Activation
5/8/2025
Find an easier way to identify and enroll eligible patients for your clinical trials with quality data and site selection.
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Sitetrove: Industry-Leading Global Investigator And Site Intelligence
1/20/2022
With over 500,000 investigators and more than 180,000 clinical trial sites spanning 185 countries, Sitetrove provides the data vital to accurately assessing target locations, identifying qualified investigators, and prioritizing candidates for clinical trial success.
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Global Compliance Made Easy
5/6/2019
Global clinical trial disclosure compliance is inherently complex, with over 39 registries, Most sponsors simply lack visibility into all the places they need to disclose information or what their commitments are. Automation can help make global compliance easier.
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Helping Sponsors Keep Up With The Latest Clinical Trials Intelligence
11/11/2022
Trialtrove helps sponsors form development strategy, anticipate competitive activity, benchmark trial designs and analyze trends. Sponsors also enjoy direct access to industry-leading analysts.
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Modernizing Clinical Research With AI And Digital Data
3/7/2025
Discover how ActiGraph is revolutionizing clinical trials with patient-focused digital data and cutting-edge technology that enhances trial efficiency across all phases.
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TMF Migrations: Streamlining The Journey To An Inspection-Ready Result
9/18/2023
Delve into several techniques designed to safeguard data precision and integrity throughout the TMF migration process, reducing compliance risks and conserving valuable time and effort.
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The Future Of Clinical Data Management: Part 1: Too Fast, Too Furious
3/23/2022
Medidata’s first webinar series for 2022 will bring industry leaders and game changers together to discuss the trends and insights in modernizing data management. This first webinar will provide best practices, practical tools and strategies that can be used today and actions to support the future "new normal". In this session, you will learn about three strategies to amp your data quality management.
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Improving The Quality Of Submitted Studies To ClinicalTrials.gov
11/7/2019
Want to reduce QC comments? Hear tips from Dr. Deborah Zarin, former director of ClinicalTrials.gov, now with the MRCT Center. Dr. Zarin was keynote speaker at the recent EXTRA: TrialScope Transparency Experience.