Alcedis - a HUMA company’s Post

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

We have been working hard to put the power of unlimited custom analytics for clinical trials at your fingertips. No matter what EDC forms, whether eCRFs, electronic PD Logs, eSAE Report Forms, ePRO questionnaires, RTSM data, or any combination thereof. All can be visualized and analyzed in real time. What type of visualizations are most useful to you? Trial tracking? Management? Primary or safety data? RBQM reports with QTLs? All of the above? Let me know in your comments.

Building a great electronic case report form enables you to deliver the highest quality data & speed time to capture, and starts with understanding the anatomy of one. Learn it here to drive clinical trial success: https://bit.ly/439vxof #eCRF #ClinicalTrials

👩🔬Struggling to Streamline Your Clinical Research? Are the complexities of data collection and participant engagement hindering your clinical trials' progress? We've got you covered with tailored #eCRF solutions designed specifically to address your challenges. 🗂️   #clinicalresearch #clinicaltrials #bestpractice #innovation

With Clincase, you stay in control—easily manage your Decentralized Clinical Trials, support your patients, and keep everything running smoothly, no matter where they are. 📱 Better Engagement for Your Patients: Multilingual support, video calls, and push reminders to help keep patients on track and engaged. 🔒  Protecting Patient Privacy and Confidentiality: Onboard patients easily without storing personal identifiers like name, phone number, or email. 💊 Ensuring Better Study Medication Compliance: Push reminders help patients stay on track with self-administrable IMP, promoting adherence to the study protocol. 📊 Patient-Friendly Data Collection: Whether using our ePRO app or browser, patients can easily report medication intake, complete QoL surveys, and log adverse events. Decentralized Trials. Centralized Control. Swipe through to learn more, and schedule a demo with Monique Dugueperoux-Klocke today to experience it firsthand! https://lnkd.in/dUA4DCRn #Clincase #EDCsolutions #ePRO #ClinicalDataManagement #DecentralizedTrials #ClinicalTrials #BioTech #Innovation #DMB2024

Who is responsible for post-closeout study data? Per regulatory guidelines, it is the Sponsors’ responsibility that: “Any system where investigators enter data should be providing this data at the conclusion of a Clinical Trial”. However, when your study is closed and archived, the investigators are no longer able to access cumulative IRT data. Should a site be audited, it would not have sufficient cumulative IRT data to accurately recreate the full traceability and history of subject and kit data. Learn more: https://okt.to/6RgEC8 #clinicaltrials #clinicaldatamanagement #clinicalresearch #clinicaloperations

Join Our Webinar: The Three E's - eCRF, eConsent, and ePRO 📢 We're excited to announce our upcoming webinar, July 11 at 5 PM CET! This is a must-attend event for anyone involved in clinical trials. What You'll Learn: 📝 Streamlined Data Management: How eCRF (Electronic Case Report Forms) can simplify and ensure accurate data collection. 💬 Enhanced Patient Engagement: The role of eConsent in improving patient understanding and compliance. 📊 Improved Data Quality: The benefits of ePRO (Electronic Patient-Reported Outcomes) in capturing reliable patient data. 🚀 Operational Efficiency: The overall impact of digital solutions on the efficiency of clinical trials. Don't miss out on this opportunity to learn with Obuchinezia Anyanwu about the future of clinical trial management. 🔗 Register now to secure your spot! Obuchinezia Anyanwu https://lnkd.in/d2NcE8yQ #ClinicalTrials #eCRF #eConsent #ePRO #Webinar #DigitalHealth #HealthcareInnovation

PN Update: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification

IMPALA Webinar available: Identifying Anomalies in Clinical Trial Data with CTAS. Learn more about the open-source R Package that identifies outliers and anomalies efficiently and accurately in clinical trial time series. Visit https://ow.ly/FbG050S79bU