CRScube Inc.’s Post

More flexibility + more repeatability + more first time quality = less effort = faster timelines. Have a look below. #EDC #eCRF #eClinical #clinicaltrials #CRScube

Ready to capture high-quality data quickly and smoothly from clinical sites and participants? Prepare to build forms that will speed time to capture, enable the widest possible integration, and facilitate robust and rapid analysis. Get access to The Ultimate eCRF Design Guide for clinical trial success: https://bit.ly/3J3mrQr #OpenClinica #ClinicalTrials #eCRF #eCRFDesign

In this digital day and age, it's hard to believe that some clinical trials are still capturing data on PAPER! ✍ Think about it - clinical trials could've been recorded back when paper was first invented ~105 AD...If your current EDC is not up to the mark 🎯 or you're still stuck in the 📜 Paper Age, it's time to consider the Cloudbyz #EDC with it's 🤸♀️ flexible #eCRF building! For more details on the benefits of going digital, check out my blog - https://lnkd.in/evRNuQ4g

Attention NGS Providers Reporting Laboratory Services:CLIA Number Processing Issue National Government Services has been made aware of an issue with clinical laboratory improvement amendments (CLIA) lab claims processing. CLIA numbers were not loaded through common working file (CWF), resulting in claim denials as CLIA did not match any file. We were informed that CWF initiated a fix late last week. After testing it was identified the CLIA numbers were showing properly in CWF. Now that the issue is resolved, we’re awaiting word from CWF to identify when the issue began. Once that’s determined we’ll identify claims that denied inappropriately and work to initiate a mass adjustment for them.  You do not need to take any action however, the process of mass adjusting effected claims may take some time. If you prefer not to wait you may exercise the option to request a Large Volume Adjustment Macro (LVAM) reopening request. Visit Reopening Versus Redetermination for more information. It is not required that you request a reopening as we will adjust denied claims.

In case you missed it last week, we highlighted the importance of IRAS in helping streamline your human trials application and approvals process. 💡 Don't forget... the approvals pathway can take some time and making revisions is fairly normal. 💭 How do you prepare your applications? Head over to our Trialflare blog to learn more! 👉🏽 https://buff.ly/42XY942 #clinicaltrials #nutritionaltrials #humantrials #epro #ecrf #econsent #ctms #decentralisedclinicaltrials #trialflare

The current EDC systems pose challenges with the growing volume of data and study complexities. There is a rising demand for the EDC systems of today to be more robust, interoperable, intuitive, and interconnected to meet the future needs of #clinicaltrials. Read more: https://bit.ly/48MvujN #ClinicalResearch #Blogs #LifeSciences #IEDC

EDC - Feature of the week #14 💠 Risk-based Monitoring - Insights Part I 💠  Curious about what CRAs find most beneficial about our eCRF and how our EDC system simplifies their daily work? We asked our users for expert feedback and here are some of the answers (spoiler alert: it's about the well-structured workflow and our system's speed): 🔍 Efficient Data Verification: During eCRF setup it is already taken into account which parameters are collected and checked together. This simplifies the SDV process and makes it more efficient. ⚡ Speed: The eCRF's rapid functionality speeds up the monitoring process, enabling immediate on-site confirmations. This speed is of crucial importance, as delays can lead to errors and limit efficacy. 🎯 Precise Release: On the one hand, the system allows individual parameter release, providing an efficient workflow for risk-based monitoring. Unlike the visit-based approach of other systems, this feature increases accuracy and eliminates unnecessary documentation. On the other hand, the system also provides the flexibility to release entire sections as required. 📊 Centralised Monitoring Graphs & Notifications: Graphs and notifications tailored to a study's QTLs and KRIs are an outstanding feature, especially for complex studies. These customisable features provide a comprehensive overview for centralised monitoring as one tool for perfect sponsor oversight. Stay tuned for more insights next week... ⏰ #data #dataentry #DataManagement #Efficiency #EDC

Adding the final touch to the #EDC solution for your individual study project. ⏩ Over 20 #eCRF Plugins developed by Alcedis offer flexibility and precision for the documentation and processing of information to save time and ensure that the study is on track. ⏱️ Check out 𝘁𝗵𝗲 𝗳𝗶𝘃𝗲 𝗲𝘅𝗮𝗺𝗽𝗹𝗲𝘀 𝗯𝗲𝗹𝗼𝘄, along with our blog article, to learn more about the selection of #plugins in clinical trials and how much these tools can streamline processes. Click the following link! ➡️ https://lnkd.in/epVXgTfn #AlcedisInsights #AlcedisPlatforms #ClinicalTrials

How do you make a great SOP for clinical research? Here are some great tips to help you improve your team's performance with a to-the-point and comprehensive SOP: ⭐ Improve trust within your team ⭐ Reduce costly mistakes ⭐ Improve team confidence ⭐ Disaster Forecasting What are your steps to creating your best SOP? How often do you review them? Head over to our Trialflare blog to learn more! 👉🏽 https://buff.ly/3Suqf35 #clinicaltrials #nutritionaltrials #humantrials #epro #ecrf #econsent #ctms #decentralisedclinicaltrials #trialflare

The basics. Clinical trial softwares are changing, attends this webinar to hear about the latest innovation :)