Authors
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Managing Biospecimens in Cell and Gene Therapy TrialsPursuing new tools and capabilities in sample logistics, storage, and data analysis.
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Putting Collective Insights Into Action to Advance Cancer Care: Key Examples From ASCO 2025At ASCO 2025, clinical operations leaders gained critical insights into how AI tools, bispecific antibodies, and evolving treatment paradigms are reshaping trial design, endpoint selection, and patient stratification.
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Benchmarking the Investigative Site Qualification ProcessInsights identify opportunities to optimize sponsor, CRO, and site collaborations.
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Unleashing Their Potential: The Evolving Landscape of DHTsKey considerations in deploying fit-for-purpose digital health technologies in drug development.
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Harnessing Patient-Centered Science to Improve Health Outcomes and Commercial Pharma SuccessGood scientific principles and practices are essential for maintaining quality data that patients can benefit from.
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Scaling eSource-Enabled Clinical Trials: Hospital PerspectivesThe challenges, opportunities, and strategic outlook for oncology research centers.
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Build Relationships with HCPs to Reach Potential Clinical Trial PatientsIncreased outreach is necessary to combat poor recruitment and large focus on patients near study centers.
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Clinical Trials and TrustUnderstanding the role of social determinants on clinical trial participation and trust.
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Future of Clinical Trial Documentation Management: eTMF Integrated with BlockchaineTMF-blockchain technology offers a myriad of application benefits to data quality and integrity while ensuring compliance to ethical standards.
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Integration of Point-of-Care Devices in Clinical TrialsA look at the future of clinical trial laboratory testing amid the emerging use of new devices at the point of care.
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COVID-19 Five Years Later: The Impact on Drug DiscoveryCOVID-19 not only advanced scientific boundaries, but also transformed research methodologies and accelerated adaptive clinical trial design.
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Navigating the New World of Dermatology TrialsHow partnering with a CRO that has experience in both dermatology and innovative trial approaches can help sponsors differentiate their studies and facilitate recruitment.
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Towards Data-Driven Clinical Trial Planning and StrategyOptimizing feasibility through increased data collection.
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How One CRO Uses RBQM in DCT ImplementationIndustry provides endless methods in crafting solutions for patients.
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The Importance of NGS Panel CustomizationExplore the pivotal role of Next-Generation Sequencing (NGS) panel customization in driving advancements in oncology research.
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Rethinking ECOG Scores to Improve Patient Access and Clinical Trials EligibilityRecent study results highlight need for new metrics in ECOG scoring to mitigate variability.
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The Strategic Emergence of Site Networks in Clinical ResearchA data-fueled framework for sponsors and CROs in navigating this shifting terrain.
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The Transformation of Clinical Trials from Writing on Papyrus to the World of TechnologyNew requirements must be put in place to ensure data quality and integrity.
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Trial Site Engagement Models are Poised for DisruptionThe role of the clinical research associate may be key in addressing challenges around the adoption of digital tools.
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Managing Clinical Trials During the COVID PandemicHow one CRO in India quickly implemented processes and technology to mitigate risk
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New Technology Springs Innovation in Clinical Trials SpaceMany companies have implemented new technologies and are adopting clinical trial models that are more patient-centric.
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A Global Network to Empower Leaner Oncology Clinical Trials: Unlocking the Potential of Local Genomic Biomarker Testing in EuropeMonday, October 25, 2021 at 10am EDT Attend this webinar to hear about CGP, the latest in onco-innovation for genomic biomarker testing and uncover the role that Illumina and Q2 Solutions are playing in evolving the CGP testing landscape to deliver a localized testing model to support oncology precision medicine clinical trials in Europe. Lastly, the webinar will reveal the updated roadmap of Q2 Solutions’ Edinburgh Genomics laboratory.
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ePRO and Ensuring Data IntegrityPush for accurate data collection during pandemic led by increased focus on patient engagement.
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Real-World Use of an Artificial Intelligence-Supported Solution for Coding of Adverse Events in Clinical TrialsStudy evaluates the use of AI-supported medical coding module.
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The Value of Integrated Data Views for Clinical TrialsTo have a successful integration of data from across clinical systems, a strong understanding of the data is a critical.
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With Project Optimus, Success Favors the PreparedOncology drug developers must start asking questions in preparation of FDA’s dose optimization initiative.
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Distribution Network Ensures In-Home Trials and Patients SucceedIndustry must work closely with patients to advance the use of decentralized technology.
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The 50-Year Technology Drought in Clinical Trials: How AI Teammates Will Finally Bring Us Into the Modern EraWhy a fundamental reimagining of how clinical studies operate is still necessary to achieve a true paradigm shift—and shed the cycle of reliance on incremental gains.
