Authors
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eConsent: Why Language MattersFostering common eConsent terminologies enriches communication and understanding across all stakeholders.
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Science is Moving—Clinical Trials Must Catch UpThe importance of applying past lessons to align clinical development with scientific advancement.
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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?
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Listening at Scale and Leveraging Conversational Data to Improve Clinical RecruitmentHow can managers ensure their clinical trial participants represent future patients?
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Examining the Current Value of ClinicalTrials.gov Listings for Patients and the PublicLooking beyond regulatory compliance.
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Characterizing Clinical Data Management Challenges and Their Impact2020 Tufts CSDD – IBM Watson Health benchmarking study highlights need for new functionality from EDC solutions and providers.
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The Current Status of European Research Related to COVID-19: The EUCROF PerspectiveSuccessful collaborations between Pharma/Biotech/Device industries and CROs will play a key role in an effective fight against the global COVID-19 pandemic.
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How to Improve Recruitment Rates, Reduce Site Burden, and Avoid Wasted SpendingIn light of Facebook ban on ads targeting patients, industry has chance to reinvent digital advertising for trials.
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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.
