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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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eConsent: Why Language MattersFostering common eConsent terminologies enriches communication and understanding across all stakeholders.
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At-home Self-collection of Blood Specimens for Safety Lab Testing in Clinical Trials via the Tasso+ DeviceLaboratory services organization focuses on easing patient and site burden with improved collection device.
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The Only Thing Certain is the Uncertainty: How to Re-Plan Future Clinical Trial Enrollment in Covid-19 TimesSponsors need to develop a strategy on how to evaluate the impact of the pandemic on the re-start of halted trials.
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Shifting Expectations for Clinical DevelopmentCOVID-19 speeds up clinical research and creates new advancements within industry.
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What Stands in the Way of an Efficient CRO-Pharma Collaboration?Survey taken by CROs and pharma/biotech companies seeks answers in maximizing partnership.
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The Federal Research Credit: Is It Worth All the Trouble?The key considerations for sponsors in deciding whether to claim the credit.
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When Should the Audit Trail Begin?A discussion of the regulatory history behind audit trails and its interpretation as it relates to clinical research data originating or residing in EDC or eCOA systems.
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Alternatives to Permanent EmployeesHow pharmaceutical start-ups can mitigate risk and avoid costly hiring mistakes.
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How Pharma Needs to Prepare for the Next PandemicMaster protocols helped accelerate research during the pandemic in the EU. How can US companies learn from this and start preparing master protocols now?
