news roundup
PPD has launched a clinical research associate apprenticeship program targeting military veterans and service members with medical backgrounds who are transitioning to the civilian workforce.
The Leukemia & Lymphoma Society has selected Medidata’s Clinical Cloud platform to power its trial for acute myeloid leukemia (AML).
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IRT EUROPE – Interactive Response Technologies in Clinical Trials
4-5 April 2017 | Hilton Paddington | London, England
Leverage IRT to Enable Innovative, Flexible and Efficient Supply Chain Management for Clinical Trials
 www.cbinet.com/irteu |
Oracle Health Sciences Data Management Workbench Cloud Service enables pharmaceutical companies and CROs to integrate, reconcile and analyze the growing variety and volume of clinical and healthcare data.
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Is Your CTMS Working for You? Unify and Optimize Your Approach to Clinical Trials
Live Webcast: Wednesday, April 26 at 1:00pm EDT
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Articles
While patients are the driving force of disruption in healthcare and clinical trials, technologies that are poised to drive change include artificial intelligence, machine learning and big data.
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Improving Clinical Trial Transparency, Collaboration and Efficiencies
Live Webinar: Wednesday, March 29 at 11:00am EDT
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This peer-review paper investigates the potential differences between using mean calculated from public data only available at the study-level and median calculated from site-level data from CTMS.
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Blog Posts
Glenn Morrison, Executive Director of Clinical Development at Zogenix, discusses how biopharmaceutical enterprises can apply techniques used in oncology clinical trials in CNS development.
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Use Challenge Trials Effectively in Clinical Studies: Lessons Learned from H3N2 Influenza Virus
Live Webinar: Tuesday, March 28 at 3 pm CEST and Thursday, April 6 at 10 am EDT
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The survey will evaluate how endpoint adjudication is impacting study design, and uncover operational challenges with endpoint adjudication and endpoint adjudication outcomes. |
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RBM
This article addresses using the right mix of KRI and CSM reports to strengthen centralized monitoring activities and ensure adequate amount of monitoring of key aspects to support RBM approaches.
Justin Stark, Head and Director of Risk-Based Monitoring and Standards at UCB, discusses TransCelerate’s Interactive Guide on RBM, its RBM toolkit, and advancements in RBM.
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The ICH GCP E6 R2 puts more onus on sponsors, investigators, and CROs and requires sponsors to adopt adequate processes for monitoring trial activity, communicating across sites, and maintaining data integrity.
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Are Local IRBs Really Necessary?
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