news roundup
Sorrento Therapeutics, Inc. has signed a new agreement with OmniComm Systems, Inc. in which they will use OmniComm's TrialMaster EDC technology to develop clinical studies at multiple Sorrento research sites.
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Neuropathic Pain Studies: Patient Selection, Study Design, and Clinical Trial Challenges
Tuesday, November 6, 2018 at 11am EST | 8am PST | 4pm GMT | 5pm CET Register Now |
Partners Cmed and Innovative Physics have combined forces to showcase The Real Time Medical Imaging Users Tool Kit®, which uses artificial intelligence to support secure, rapid diagnostics in clinical trials for lung scans.
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Identifying NASH Patients: Solutions and Strategies
Thursday, November 1, 2018, 11am EST Register Now |
IQVIA announced the expansion of its alliance with Salesforce to build a clinical solution for life sciences on Salesforce Health Cloud. IQVIA's suite of clinical technology solutions was created to potentially accelerate research and trial safety, and protect patient privacy while boosting patient participation, adherence, and convenience throughout the study.
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Driving the Execution of Cannabis-Based Clinical Trials
Tuesday, October 23, 2018 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST Register Now |
Quanticate has announced that it has partnered with CluePoints as part of its new Data Quality Oversight service. This partnership will allow Quanticate to offer its customers the creation of statistical analytics reports on key risk indicators and comprehensive risk signals across all clinical and operational data.
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A Pan-cancer View of Immune Cell Activity, Immune Checkpoints, and Tumor Mutational Burden
Thursday, October 11, 2018 at 11am EDT
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On the brink of change: How academic data and machine learning can revolutionize Alzheimer's drug development
Thursday, October 4, 2018 at 11am EDT
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Research Reveals Data Quality Issues Slow Clinical Trial Progression – What Can You Do To Prevent This?
Wednesday, October 3, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
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Artificial Intelligence: A Transformative Journey for Pharmacovigilance
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Challenging the Status Quo: The Diffusion of Technology in Study Startup
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A Next Generation Sequencing Approach to Influenza Vaccine Development
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Decoding the Distinction: DMCs, CECs, and Their Role in Medical Device Research
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Articles
Data integrity is the essence of GMP, the cornerstone of how the industry operates, and it is vital that all organizations embrace it to survive the rapidly changing life sciences landscape.
These seven key building blocks for success are outlined to help companies develop and implement a data-and-analytics-driven approach to clinical trial feasibility.
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Blog Posts
There have been a number of significant scientific and regulatory milestones driving the adoption of electronic patient-reported outcomes in clinical trials since the first screen-based ePRO solution, Minidoc, appeared in 1980.
The workings of the European Union are notoriously complicated, with the result that misunderstanding is commonplace, even among those who might like to know more about it.
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