news roundup
CluePoints will work with the Metrics Champion Consortium to help drive collaboration in the development of a standardized framework for centralized monitoring.
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 Click here and press play in our video player to watch a short video about Covance's Xcellerate Monitoring solution, to help you prioritize patient safety and data quality, support protocol compliance, and optimize resource utilization.
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Certification of hospitals in Turkey, with access to 27.5 million potential study participants, aims to speed overall recruitment and advance patient engagement.
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Podcast: E-Signatures and Digital Workflows in Clinical Trials
In clinical trials, the use of eSignatures to improve document workflows such as protocols, informed consent, and investigator brochures, has increased. All documents that need signed approvals eSignatures can be implemented to streamline, improve and make the transferring of those documents more efficient. This podcast discusses areas in clinical trials where eSignatures and document workflow can be applied for upstream benefits. Click here to Listen
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The Patient Preferences in Benefit-Risk Assessments during the Drug Life Cycle (PREFER) five-year project will assess how to best include patient-preference in decision making.
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The Evolution of Regulatory Affairs
Live Webinar: Wednesday, December 7 at 11:00am EST
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Articles
Perhaps one of the largest challenges for organizations has been benchmarking multi-company performance, efficiency and quality metrics.
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The Next Wave of Centralized Monitoring
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Michael Sweeney, senior director of global service development at World Courier, and Stuart Redding, vice president of global business development and marketing at MRN, share insights on the evolution of community-based trials.
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Vendor Overload? Integrating third party lab management to streamline clinical development
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Blog Posts
Trial sponsors and CROs can expect plenty of tough questions to be posed about whether their current technology platform can really support the next iteration of RBM.
Collaborative with Michael J. Fox Foundation, RTI Health and others will evaluate patient benefit risk preferences throughout a product's lifecycle.
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Oncology
The Leukemia & Lymphoma Society (LLS) announced its Beat AML Master Trial that involves a number of cancer centers, as well as INC Research as its CRO and myClin as its clinical trial knowledge platform.
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Continuous Glucose Monitoring (CGM) in Clinical Trials: An Evolving Regulatory Landscape
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Schulman IRB will launch its new Central Oncology Review (COR) division this month. The COR will feature a roster of oncology industry leaders, academics and scientists, each with a background in managing specialized oncology research.
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Regulatory Changes in India and What It Means for Clinical Research in the Country
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Small and mid-sized biopharmaceutical companies play significant, pioneering roles in creating new immunotherapies. However, because such sponsors typically have limited resources, they often require outsourcing support to plan, launch and manage clinical investigations.
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Simplifying the complexities of global rare disease drug development
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While not solely for oncology patients, new technologies and solutions do increasingly target a personalized approach to matching patients to trials.
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