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Harnessing the Power of Scientific SurveillanceStatistical methods used via this technique in centralized monitoring.
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Demystifying Submissions of eCOA Documentation for Ethics Review: Are We Making Submissions More Difficult than Necessary?Examining how to optimizing the time and effort of Ethics Committees to efficiently and effectively fulfill their human subjects protection remit.
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Clinical Trials are Getting More Diverse Thanks to AI—and HumansStrategies for sponsors to utilize technology in reaching diverse patient populations.
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Optimizing Technology Implementation to Improve Diversity in Clinical ResearchThree key considerations for deploying technology to help increase diversity in trials.
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Understanding the Complexities of Diversifying Clinical TrialsTufts Center for the Study of Drug Development and Biogen recently conducted a study to inform growing interest in improving diversity of clinical trial participation. The results of this research provide insights into increasing the community of minority investigators and study staff and presenting greater access to clinical trials among minority study volunteers.
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Accelerating Clinical Trial Design and OperationsFully-integrated, component-based CDMS offers flexibility, customization, and efficiency.
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The Backbone of Innovation: High Quality DatasetsUnderstanding the benefits and concerns associated with implementing datasets into clinical trial workflows.
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Towards Data-Driven Clinical Trial Planning and StrategyOptimizing feasibility through increased data collection.
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Engaging Emerging Clinical Investigators Yields Unique Benefits for AllNew investigators practicing in community-based settings bring enthusiasm and a fresh approach to clinical research, while also boosting collaboration and merging personal connection and patient-centric insights.
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How Life Sciences Companies Can Strengthen Regulatory Submissions With External Control ArmsData from past clinical trials has provided researchers with a good starting point to create more ECAs.
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Decentralized Clinical Trials Bring Research to the Patient—in More Ways Than OneDCTs proving to solve numerous pain points for patients in clinical research.
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Optimizing Technology Implementation to Improve Diversity in Clinical ResearchThree key considerations for deploying technology to help increase diversity in trials.
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Tips to Rescue a Clinical Trial Before It’s Too LateWhy constant communication and transparency are paramount to successful partnerships between pharmaceutical companies and CROs
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Virtual Clinical Trials Post-COVID-19: Collaboration Will Be Key to SuccessThe use of virtual trials will surge in the future and could become the de facto standard for clinical studies, says a recent Pistoia Alliance poll.
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The EU Regulations Catching US Pharma Companies Off GuardCompanies that understand the regulatory environment in Europe can keep their trials on budget and on schedule.
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Changing the Paradigm in AI ImplementationHow pharma companies can reduce the risk of failure with AI-based innovations.
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Putting Labeling on the Boardroom AgendaHow smart packaging can aid clinical trial adherence.
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Using Clinical Trial Sites' Input to Select the Right Capabilities when Decentralizing Clinical TrialsThis paper analyses the responses from more than 800 US-based clinical trial sites to understand their decentralized clinical trial capabilities and perceptions
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Adapting Site Selection for Clinical Trial Decentralization and the Future LandscapeSites not expected to fade away even as DCTs continue to grow past COVID-19.
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Harnessing Unstructured Data and Hospital InteroperabilityThe potential of next-generation platforms in transforming patient recruitment.
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How Clinical Trial Research Sites Can Gain Access to a More Level Playing FieldTo overcome sponsor-related challenges and work to successfully secure more trials, there are tactical steps CROs can take.
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Modernizing Data Management in the D-Clinical Age***Live: December 9, 2020, at 11am EST| 8am PST| 4pm GMT| 5pm CET*** In this ‘D-Clinical Age’, leveraging modern technologies and new approaches and mind sets is required to accelerate the development of new treatments. This webinar will examine how data management can drive digital transformation with the right mix of technology, skills and process redesign.***On demand available after airing until Dec. 9, 2021.***
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Demystifying Submissions of eCOA Documentation for Ethics Review: Are We Making Submissions More Difficult than Necessary?Examining how to optimizing the time and effort of Ethics Committees to efficiently and effectively fulfill their human subjects protection remit.
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Designing Cell Therapies to Target Solid TumorsA look at one company’s platform approach in enabling the engineering of T-cells to identify and destroy cancer.
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DPHARM 2024: Developing AI/ML Models for Clinical TrialsIn an interview with Nico Saraceno at DPHARM 2024, Munther Baara, VP strategy and innovation, EDETEK touches on the features an effective AI/ML model can provide and how they benefit data management in trials.
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Clinical Trial Failure: A Data-Driven Perspective on Risk MitigationAn increase in protocol complexity is paving the way for machine learning models to optimize trial design.
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Considerations for the Effective Rollout of DCTs at a Global ScaleFor effective rollout on a global scale, sponsors must address and develop a plan around known challenges including recruitment, sit adoption, and technology integration.
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Powering Clinical Operations With Knowledge Graphs and LLMs With Merck KGaA, Darmstadt, GermanyWebinar Date/Time: Thu, Mar 13, 2025 11:00 AM EDT
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Regulatory Data: How Technology Can Help ClinOps SurviveClinical operations professionals, burdened by lack of data standardization, turn to technology in hopes of streamlining regulatory processes for the future.
