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Animated Explainers Can Be Game-Changers in Cohort RecruitmentBy using engaging visuals, researchers and companies can better communicate complex concepts, increase trial participation, and foster public trust in science.
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How to Address—and Overcome—Operational Challenges in Master Protocol StudiesTrials that address multiple questions simultaneously using a master protocol can be operationally complicated. These complexities can be managed, even in studies used to support a marketing application.
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Enhancing Care and Research: Digital Technology's Impact on Rett Syndrome ManagementWearables have great potential to continue advancing research in Rett syndrome as well as other rare disease areas.
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Turning Challenges into Opportunities: Evaluation of Digital Health ProductsShiri Diskin, PhD, Head of Medical Writing at Bioforum, sits down with Daphna Laifenfeld, PhD, Chief Scientific Officer at Ibex Medical Analytics to discuss the challenges associated with developing a CER and how to effectively navigate them while creating opportunities that increase efficiencies.
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Improving Clinical Trial Patient Diversity: Can Central Imaging Play a Role?Centralized medical imaging providers must challenge their current processes to improve patient diversity.
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Accelerating the Progress of Kinase Inhibitors in OncologyThe potential of PBPK modeling in answering key questions around these drugs.
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AiCure Overview Fact SheetModern clinical trials can be an overwhelming experience for participants, compromising everything from medication adherence and data quality to overall study outcomes. AiCure’s H.Code is a patient engagement platform that reinvents the clinical trial experience for participants using cutting-edge AI, easy communication, and dedicated support for sites. Read our fact sheet to learn how H.Code extends the reach of your clinical team using an AI-powered analytics platform and a user-friendly smartphone app.
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Accelerate Clinical Trial Success with Genomics ExpertsWebinar Date/Time: Thu, Mar 2, 2023 1:00 PM EST
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Improving Diversity in Clinical TrialsEmploying a Multi-faceted Approach to Cultivate Inclusivity and Close Disparity.
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Streamlining Clinical Trials with eSource: Insights from MSKA use case by Memorial Sloan Kettering Cancer Center explores the potential of EHR-to-EDC.
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Innovations in Data Capture Transforming Trial DeliveryAdvances in technology open door for improved EHR to EDC transfer process.
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Considerations to Reach Underrepresented GroupsRegulatory compliance, collaboration, and effective use of technology among ways CROs can overcome challenges.
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Notable Discussions from SCOPE 2025: Aiming to Calculate, Accommodate, and Innovate for Enhanced Drug DevelopmentThis year’s conference highlighted a number of critical areas in clinical R&D including financial management, representation, and eCOA.
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Benchmarking the Investigative Site Qualification ProcessInsights identify opportunities to optimize sponsor, CRO, and site collaborations.
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3 Ways to Turn Client Experience into Your Competitive Advantage*** Thursday, March 11, 2021 at 11am EST | 8am PST | 4pm GMT | 5pm CET *** How can CROs continue to grow in today’s increasingly competitive market? Learn how you can turn client experience into your competitive advantage. *** On demand available after final airing until Mar. 11, 2022 ***
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Opportunities for Improving Clinical Decisions with Patient Centric Remote Blood Sampling ApproachesThis article sets out a vision of adopting convenient alternative blood sampling approaches that places the needs of the patient at the center and enables active monitoring, before the onset of clinical events, leading to improved healthcare.
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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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Prioritizing Patients: Strategies and eCOA Best Practices in Drug DevelopmentA more user-centered design can allow increased flexibility in the development of eCOA platforms, driving better engagement and participation.
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Central RBM Supports Reduced Cost, Higher Data QualityImplementing centralized risk-based monitoring can help meet strict GCP requirements for study conduct, oversight, and recording.
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What the Future of Study Review Processes Should Look LikeInsights from Bayer’s study review process showcases importance of incorporating feedback from a wider audience of stakeholders.
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Four-Steps to Accelerate Study Start-up CyclesIdentifying KPIs, benchmarks, key data points, and an actionable plan are all keys to accelerating study start-up cycles.
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How Today’s Digitally Driven Research Could Drive CAR T-cell Therapy Protocols of the FutureNew protocols, remote patient monitoring, and improved standards of care among ways industry can take next steps in CAR T-cell research.
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What Patients Expect from Clinical Trials in the COVID-19 EraKey takeaways from a survey of 250 oncology patients measuring COVID-19’s impact on patient willingness to participate in clinical trials.
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Targeting Patient PopulationKeys to ensuring your clinical trials better reflect your target population.
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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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How to Address—and Overcome—Operational Challenges in Master Protocol StudiesTrials that address multiple questions simultaneously using a master protocol can be operationally complicated. These complexities can be managed, even in studies used to support a marketing application.
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Enhancing Clinical Trial FlexibilityAs drug development costs continue to escalate, sponsors are incentivized to find less expensive approaches to develop their assets. FSP models provide increased operational and resourcing flexibility and different pricing plans in comparison to traditional full-service CRO offerings.
