Bringing Web3 to medical research by developing blockchain-integrated software solutions for clinical trials | $TRL | Telegram: https://xitter.cf/t.co/rQL2IvaJcR

Amsterdam, The Netherlands
Joined July 2018
Triall and MayoClinic to advance blockchain technology in clinical trials We are proud to share that @MayoClinic will onboard Triall's #blockchain-integrated #eClinical platform in a #clinicaltrial that includes 10 sites and 500+ patients across the US. finance.yahoo.com/triall-adv…
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LBank de-listing announcement In light of Triall’s company closing, $TRL will be de-listed from @LBank_Exchange at 12:00 UTC on March 4, 2024. Please cancel your pending orders. For those who do not actively cancel, LBank will cancel them uniformly. support.lbank.com/hc/en-gb/a…
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MEXC de-listing announcement 📢 In light of Triall’s company closing, $TRL will be de-listed from @MEXC_Official on March 2, 2024. Please withdraw your assets in time to avoid any asset losses. 👇 More info on deposits, trading, and withdrawals: mexc.com/support/articles/17…
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Community announcement 📢 Dear Triall community, It is with a heavy heart that we must inform you about challenges Triall is facing in light of ongoing economic headwinds. 👉 Read the full message: t.me/triallofficial/590
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#TRLInsights - 55% of sponsors & CROs report using RBQM in their #clinicaltrials. 78% trust that #RBQM improves study quality, while 64% believe RBQM increases efficiency & cost savings, and 53% trust it can reduce timelines. Source: csdd.tufts.edu/impact-report… #DeSci #TRL
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5 key areas for reporting & analytics in clinical trials 👩‍💻 eClinical tech continues to open up new avenues for reporting & analytics, promoting #clinicaltrial quality, efficiency & adaptability. 👇🧵Here are 5 critical areas for reporting & analytics enabled by #eClinical:
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🌐 Custom reports & integrations eClinical platforms have evolved to support the creation of custom reports & dashboards. Additionally, a growing body of eClinical solutions offer seamless #API integration with other internal systems and #BI tools, further boosting visibility.
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And that's a wrap! Want to empower your studies with the latest reporting & analytics features? Our eClinical platform supports all of these 5 capabilities. Reach out to our team at [email protected] for more info. #blockchainforhealth #TRL #DeSci
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#TRLInsights - According to @TuftsCSDD, a typical Phase III #clinicaltrial conducted during 2016-2021 included an average of 25.8 endpoints. This number is 37% higher compared to 2015, signalling a sharp increase in clinical trial complexity. Source: csdd.tufts.edu/impact-report…
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#TRLInsights - 1 in 3 participants do not feel valued for their contribution to clinical research. This can impact retention, satisfaction & overall adherence. @TranscelerateB has therefore developed a best practices #Gratitude #Toolkit. 👉 Source: transceleratebiopharmainc.co…
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⏩ Auto-validation ⏩ Study builders are increasingly using auto-validation simulators to validate their eCRFs against preprogrammed edit checks. This ensures data does not need to be entered by hand and often also auto-generates validation reports for future reference.
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⏩ Payments ⏩ Sites and participants often need to wait months before being compensated. Modern eClinical platforms tackle this issue by enabling automated payments based on completed study tasks & milestones, ensuring accurate & timely payment of key contributors.
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And that’s a wrap! Want to future-proof your clinical trials? Our eClinical platform supports all of the above workflow automation capabilities. Reach out to our team at [email protected] for more info. #blockchainforhealth #TRL #DeSci
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⏩ Direct data capture ⏩ Solutions such as eSource, ePRO, eConsent, and wearables allow data to directly flow into the EDC database. This eliminates the need to manually transcribe data from a paper chart or EHR, thereby promoting speed and lowering #SDV requirements.
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⏩ Cross-form edit checks ⏩ A unified eClinical platform brings various interoperability benefits. Notably, edit-checks between forms (e.g., eConsent form & eCRF) can trigger edit-checks and other conditional actions that help ensure accuracy, completeness, and consistency.
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5 key automations in clinical trials 🤖 One of the most promising benefits of modern #eClinical solutions is their power to #automate manual, time-consuming, and error-prone study tasks. 👇🧵 Here are 5 promising areas for workflow automation in #clinicaltrials and #DeSci:
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⏩ Review workflows ⏩ Modern eClinical platforms enable review & sign-off workflows on a site, subject, visit, or data field-level. These workflows act as compliance stage-gates and promote efficiency by automatically notifying study monitors, data managers, and investigators.
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