About Medidata Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. PROMETRIKA’s Head of Clinical Operations, Ms. globaleducation@3ds. Medidata eConsent是一种新型临床试验电子知情同意系统，符合监管规范，便于患者使用。. Any Rave EDC studies not using eCOA can add eCOA to the project and immediately begin converting forms to remote-enabled forms. Medidata Rave eConsent: Consenting a Subject. Driving continuous innovation and the user experience is at the heart of Medidata’s DNA. Any attempts to record training will result in an immediate stoppage of training until recording is terminated. ImagingAmencefs LLC is a dedicated Contract Research Organization (CRO) that provides Data Management and EDC Programming service to Biotech and Pharmaceutical companies. FACT SHEET Rave Wearable Sensors. Available Certifications. I forgot my username or password Activate pending account. eConsent. Eliminate complex, manual processes & achieve higher quality data for faster insights. Companion. 1. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. SCTU successfully transitioned its paper and manual processes to 100% electronic data capture. Data ingestion capabilities to enable rapid ingestion, normalization, and. Global Nav Open Menu Global Nav Close Menu AppleClaim eAdjudication and update features and information. Companion. Trials using paper and hybrid data collection tools are in massive decline and this decline is expected to continue. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. Discover more at and follow us @medidata, The Operating System for Life Sciences. Medidata Rave is TFS’ preferred EDC system based on its demonstrated ability to streamline the data management process. Medidata MEDS Reporter: Getting Started. Medidata CTMS vs RealTime-CTMS. 0 Release. Rave Data Management. Now we will see how to Download Medidata Rave RCM for PC Windows 11 or 10 or 8 or 7 laptop using NoxPlayer. 43%. The Medidata DCT Program is a scalable, flexible, and comprehensive technology solution to virtualize as much or as little of a clinical trial as needed, including patient participation, data capture and management, monitoring and analysis, and supply dispensation. eConsent. Equip your clinical trial study with fast, accurate medical coding. Rave eCOA is built on the Medidata Rave Clinical Cloud's unified data platform, which enables a single source of truth for all study-related dataRave Data Management. 21%. Equip your clinical trial study with fast, accurate medical coding. 9am – 6pm KST (Monday – Friday) Mandarin. APAC. Download our latest Demo Video and to see how Medidata Rave EDC, Rave Companion solutions work under an all-in-one unified system. Rave EDC is at the heart of Medidata’s unified solution for Clinical Data Capture and Management, enabling aggregation and reconciliation of data from multiple sources – Medidata eConsent, Medidata eCOA,. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. eConsent. We use the most advanced technologies and techniques to protect data against the newest cyber threats. Rave Coder+ features ‘Code with Confidence’ 3 –. Exploratory. com eLearnings New courses are now available via iMedidata. 0 Release Training. All on any network and any device. A patient-friendly. Speaker (s) 2:00 – 5:00 PM CT. Medidata Rave eConsent: Navigating the Mobile App eLearning Course Outline Course Description: This course is designed for study managers, site users, and administrators who support or manage Rave eConsent studies. TM. Sensor Cloud. av FACT SHEET Rave EDC One Place to Capture, Manage, Clean and Report Clinical Research Data Rave EDC (Electronic Data Capture) is the most advanced and robust. Medidata, a Dassault Systèmes company (Euronext Paris: #13065, DSY. Make data entry easier and faster for sites. RAVE eCONSENT eConsent Reduces Burden and Risk Sites report a significant decrease in the administration burden for managing the consent process, handling reconsent, and. Medidata has paved the way for the next generation of clinical trials including specialized solutions like decentralized clinical trials, patient-centric solutions, synthetic control arm studies, and advanced analytics. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. Coder. 2. Medidata Global Education announces the following New and Updated Materials for October 2022. All are driven by Medidata’s PICAS database, the. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. eCOA Studies Across Regions. The key findings from. Rave CTMS (Clinical Trial Management System) improves speed and efficiency for the oversight of studies, countries, and sites through intelligent automation and workflow management. TM &Ood-aed na re earF oton nnoate tenoo ata-dren anat ed ed ot proYed te to arke t a ter deon ned rk. Coder. Coder. Medidata Remote Monitoring is a holistic, innovative digital solution to enable a flexible on-site/off-site approach to study oversight. Potential participants gain full disclosure of the nature of the research and their involvement by viewing interactive. Rave Companion dramatically reduces the time trial sites spend keying in data and resolving queries so they. 1. Medidata Rave RTSM: 2020. As a cloud-based solution accessible 24/7, Rave RTSM offers a choice of pre-New York – March 23 2023 – Medidata, a Dassault Systèmes company, launched Rave EDC Certified Study Builder certification, a new offering in its global education program for study build and study management professionals. Medidata’s Patient Cloud is a suite of products including: Rave eConsent, Rave eCOA, Rave Wearable Sensors, and Rave Virtual Trials. 2 Release Training. Integrated Evidence. This training covers key enhancements necessary to implement and support Rave RTSM successfully. 0 Release Training. com | +1 866 515 6044. Video will be available in the Rave EDC Video Library on 14/Nov/2022. These three solutions required a rapid response and significantly. Eliminate complex, manual processes & achieve higher quality data for faster insights. We, Medidata, use cookies to give you the best experience on our websites by:. Attendees will learn how to use the mobile app to: • Add a new subject • Review and clear document flagsThe naming will solely depend on what the vendor decides to call it, for example Medidata Rave RTSM, Medpace ClinTrak IRT, or ITclinical IRT:IWRS. ConclusionsOverview. Coder+Medidata Global Education announces the following New and Updated Materials for September 2023. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. We, Medidata, use cookies to give you the best experience on our websites by: measuring their audience. Apr 29, 2021 - 2 min read. , EHR – electronic health record) or document (e. AUDIENCE: Principal Investigators. Today’s clinical trials have access to various data sources, expanding beyond site-based data collection methods to remotely collected, digitized data. Eliminate complex, manual processes & achieve higher quality data for faster insights. Attendees will learn: What is eConsent? The components of the Rave eConsent solution. Sensor Cloud. The Foundation of theMedidata Clinical Cloud ®. Rave EDC. Rave EDC study using eCOA can have additional data forms pulled into the eCOA app and made available to patients. Data ingestion capabilities to enable rapid ingestion, normalization, and analysis of patient data. This app had been rated by 6 users. 0 Release Training. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. Companion. Rave Clinical Trial Financial Management (CTFM) is a suite of solutions, including Rave Grants Manager (Planning and Contracting) and Rave Site Payments, paired with the industry-leading Rave EDC. Any attempts to record training will result in an immediate stoppage of training until recording is terminated. Medidata MEDS Reporter: Report Offerings. Know more with scenario modeling based on your parameters. Companion. The industry’s. Here is the Download link for you – NoxPlayer Website. eConsent, Direct Data Capture, and Randomization and Trial Supply Management (RTSM). Rave EDC. eConsent. Transform End of Study Data Exchange. Sep 19, 2023 - 4 min read. Rave Data Management. Learn More. Topics include an overview of what to expect on exam day, a review of the various question-types included in the exam, and a refresher on the topics covered on the exam. 50% Small-Business;Built on the Medidata Rave Clinical Cloud™, Rave eCOA provides data managers with single-source, real-time data access, which accelerates database. Medidata’s Rave eConsent, electronic informed consent technology, can track individual consent and ensure the correct version of the consent is signed and dated by patients across all sites. Potential participants gain full disclosure of the nature of the research and their involvement by viewing interactive tools and animations that be…Medidata eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. A patient-friendly enrollment solution enabling patients to. eLearning. Phase 3. Medidata eConsent. Potential participants gain full disclosure of the nature of the research and their involvement by viewing interactive tools and animations that be…Medidata Rave Data Management解决方案用于临床数据管理和临床数据采集， 消除复杂的手动流程，并提供更高质量的数据以完成更快洞察。. Track/Subtrack. Description: This offering provides the eLearning courses and other. Rave Imaging, built on the Medidata Unified Platform, processes more. Rave eConsent Features and Benefits. Medidata Patient Cloud Rave eConsent is our innovative, patient-friendly electronic informed consent and patient enrollment system for clinical trials. info@medidata. Commercial Data Solutions. Coder. 0、CSS 2. Why Medidata eCOA? Rave is eCOA. The study initially focused on the countries in the European geographic region, where Medidata engaged EU regulatory authorities and industry trade associations on the concerns using eConsent. A Medidata application accessed from iMedidata. Medidata MEDS Reporter: Report Offerings. com | +1 866 515 6044. Nearly. Coder+. The awards recognize biopharmaceutical, medical device companies, and contract research organizations. Sep 25, 2023 - 2 min read. Built for patients, by patients, myMedidata is a single destination patient portal, allowing patients to use any online device to virtually learn, enroll and engage in clinical trials. The Medidata Clinical Cloud ®. Rave Coder+ is part of Medidata’s unified solution for Clinical Data Management on the Medidata Clinical Cloud ®, enabling aggregation and reconciliation of data from multiple sources – Rave EDC, Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; and intelligent data review and analysis with Rave TSDV. Any Rave EDC studies not using eCOA can add eCOA to the project and immediately begin converting forms to remote-enabled forms. Medidata’s Rave EDC and Rave RTSM were selected to support this program, and due to the recent increase in need for more hygienic processes, Medidata’s Rave eConsent was also included to consent the patients electronically using an iPad as opposed to traditional paper forms. Rave eConsent Features and Benefits. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. Coder. November 21, 2023. If you have any questions about a course’s content, please feel free to reach out to us at medidata. You will thrive in a high energy environment and be motivated to help us solve the impossible. If you have any questions about a course’s content, please feel free to reach out to us at medidata. PA), Medidata is headquartered in New York City and has been. eLearning Mapping Management. Recording of Global Education training sessions is strictly prohibited. This recognition is the latest in a long list of accolades. eConsent. Learn about Medidata’s Unified Protection strategy that encompasses secure, stable, and scalable cloud platform, robust data governance processes, and an inspection-ready quality management system. New York – October 7, 2021-- Medidata, a Dassault Systèmes company, today announced the launch of Medidata Link at NEXT Global 2021. It speeds startup and guarantees remote consent monitoring, and site screening metrics with the flexibility to meet global requirements. Medidata Rave Safety Gateway 2020. Medidata’s eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. DesignedeConsent. eLearning Course Outline. Potential participants gain full disclosure of the nature of the research and their involvement by viewing interactive tools and animations that better explain the risks and benefits of the. Rave Data Management. 13%. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. Rave EDC is at the heart of Medidata’s unified solution for Clinical Data Capture and Management, enabling aggregation and reconciliation of data from multiple sources – Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging and Sensor Cloud; and intelligent data review and analysis with Rave TSDV and Medidata. FACT SHEET RAVE eCOA 3. Rave TSDV is Medidata’s targeted SDV in clinical trials solution, empowering clinical research associates to take a risk-based approach to monitoring by focusing on critical data. Sensor Cloud. Make data entry easier and faster for sites. Intensive resources are used to capture patient data, collect study data, and monitor progress throughout a clinical trial. g. 0 Release Training. RTSM is built on Rave EDC, so there is no double data entry and minimal reconciliation expediting study start-up and study-close out. MEDIDATA RAVE CLINICAL CLOUD 介绍 2 以下是更新的解决方案称： 临床试验流程各阶段 旧名称 新名称 备注 试验执行 Rave EDC Rave EDC 临床和实验室数据 试验执行 Rave RTSM Rave RTSM 随机和临床试验供应管理 试验执行 Rave eCOA/ePRO Rave eCOA 移动. Rave Data Management is focusing on five main areas of innovation, starting with protocol-driven study design. Data ingestion capabilities to enable rapid ingestion, normalization, and analysis of patient data. eConsent. Overview. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. Boston Scientific Uses Medidata’s eConsent in Medical Device Clinical Trials Video SeriesMedidata’s AI-powered Trial Design Mitigates Risks for Faster Breakthroughs. eConsent. . This video offers a brief overview of how to manage EOS workflows, post access provision reports, and update sponsor user roles to have power user access. Connected Patient Platform. As the industry’s only unified platform dedicated to clinical research, we help life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. Medidata, a Dassault Systèmes company, is leading the digital transformation of. Medidata Study Builds Accelerate Study Start-Ups. Medidata Rave eCOA Release Training (R06 2020) Medidata Rave 2020. com | medidata. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. Over the past year, clinical trials have had to become more modernised because of the strange environment we were operating in. Rave eConsent is Free Medical app, developed by Medidata Solutions Worldwide. Using video eConsent, the patient consent process is further. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. 4 Certified Study Administrator Medidata Solutions Medidata Rave 5. APAC. Data ingestion capabilities to enable rapid. The evolution in automated medical coding for Rave EDC. Capture and manage your patient, site and lab in the most advanced, robust and secure electronic data capture system. Medidata RACT: 2019. Equip your clinical trial study with fast, accurate medical coding. with the eConsent form3 75% reduction in data clarification forms following unified Rave eCOA and Rave EDC adoption5 100%. 1 Release Training. globaleducation@3ds. Medidata Rave Study Design and Build Essentials (SDBE) – eCOA. Time. With myMedidata eConsent, patients can remotely access the. Medidata Rave eConsent: Patient Experience. 25%. Medidata eConsent は、治験の目的、リスク、利益、責任に関する理解を深めながら、患者のコンプライアンスとリテンションを向上させます。 当社の患者クラウド専用ヘルプデスクは、お客様が最も必要とする時に、最も必要とする方法で、治験施設と患者の. Attendees will learn: • The data integration workflow in Rave EDC; • What data types can appear in Rave EDC;Rave EDC study using eCOA can have additional data forms pulled into the eCOA app and made available to patients. Rave Data Management. Phase 4. To date, Rave EDC has had over 262,000 certified site users, providing a veritable treasure trove of user-generated critiques and solutions. Currently, our iPad based consent is not set up for BYOD with a patient device. Rave EDC. facing solutions for electronic patient consent (eConsent) and clinical outcomes assessment (eCOA), collection of critical data. Impact to Medidata Customers, Patients and Trials Real-time and detailed reporting and analytics are critical for sponsors and CROs to assess the day-to-day impact of the pandemic on a trial at the patient, site and country level and so they can quickly implement changes to mitigate the risk ofRave EDC, is the industry’s leading electronic data capture and management solution, offers fast implementation and maximum control to support studies of any size, length, and/or complexity. Latest version of Rave eConsent is 2022. Eliminate complex, manual processes & achieve higher quality data for faster insights. Coder. Each site completes study electronic case report forms (eCRFs) by entering data into the Medidata Rave study database. Medidata Study Management: Service Provider Tracking Overview. I. Rave EDC vs. Sites. We are dedicated to supporting the delivery of. Medidata’s Rave eConsent, electronic informed consent technology, can track individual consent and ensure the correct version of the consent is signed and dated by patients across all sites. Any attempts to record training will result in an immediate stoppage of training until recording is terminated. Rave Companion dramatically reduces the time trial sites spend keying in data and resolving queries so they. Contact Sales; Contact Support. myMedidata. Make data entry easier and faster for sites. Cancer is the leading cause of death worldwide, accounting for nearly 10 million fatalities in 2020. eConsent. Rave EDC is at the heart of Medidata’s unified solution for Clinical Data Management, enabling aggregation and reconciliation of data from multiple sources – Medidata. Sensor Cloud. Equip your clinical trial study with fast, accurate medical coding. ImagingMedidata Rave eConsent: Data Integration. 1. Powered by a unified platform, Medidata’s. Medidata’s eConsent is an innovative, regulatory-compliant, patient-friendly, electronic consent system for clinical trials. 2 Release Training. Rave EDC. This course covers new features and enhancements for Rave modules, including Web Services, Reporter, Rave EDC, Architect, ALS, PDF Generator, and more. Medical Device Clinical Trials: What You Need to Know. Compare price, features, and reviews of the software side-by-side to make the best choice for your business. Eliminate complex, manual processes & achieve higher quality data for faster insights. Rave EDC offered a robust platform to manage data from EDC and make it. Virtual Trials. We would like to show you a description here but the site won’t allow us. ImagingCompare Rave CTMS vs. Equip your clinical trial study with fast, accurate medical coding. com | +1 866 515 6044. Medidata Patient Cloud Rave eConsent is our innovative, patient-friendly electronic informed consent and patient enrollment system for clinical trials. com | +1 866 515 6044. As the leader in the digital transformation of life sciences, Medidata is proud to earn recognition for its products, programs, and people. com eLearnings New courses are now available via iMedidata. Currently our iPad based consent is not set up for BYOD with a patient device. The evolution in automated medical coding for Rave EDC. Potential participants gain full disclosure. Give your patients access to a modern digital consent. According to Medidata, Rave Omics is designed to. For people saying that this is the best system out there - that’s wrong. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. Sastry is also the Founder & President of Medidata AI, Medidata’s Data Science business. If your company is looking to adopt a new eCOA solution or. RTSM, Medidata eCOA, Medidata eConsent, Rave Imaging), or an external system connected to the Medidata Clinical Cloud, is automatically available. Medidata CTMS vs Fusion eClinical Suite. Anchored by Medidata Rave Clinical Cloud, our suite of tools is designed to help sponsors, sites, and CROs empower and engage patients at every stage of the study. Recording of Global Education training sessions is strictly prohibited. Data ingestion capabilities to enable rapid ingestion, normalization, and analysis of patient data. Compare price, features, and reviews of the software side-by-side to make the best choice for your business. Unique to the industry, the myMedidata app is unified with the Medidata Platform, including Rave EDC (electronic data capture), resulting in an entirely self-sustaining ecosystem where patient input, site based. Coder+. Rave Companion reduces clinical trial data entry efforts for sites by making it simpler and faster to get source data from any system (e. Over time, we’ve grown to be the leader in clinical technology, with thousands of people working towards the same goal: using the latest technology. PasswordMedidata's RTSM solution is a truly dynamic and flexible solution that allows end users to experience all the benefits of a RTSM with data in one place on a truly unified platform. Potential participants gain full disclosure of the nature of the research and their involvement by viewing interactive tools and animations that better explain the risks and benefits of the. A patient-friendly enrollment solution enabling patients to understand trial objectives & consent remotely. iMedidata: 2020. Medidata AI Integrated Evidence connects historical data from more than 23,000 cross-sponsor clinical trials and 7 million patient volunteers with real world data to deliver powerful insights and the necessary evidence clinical development leaders need to increase the probability of trial success. Medidata Rave eConsent: Data Integration. This improvement in patient education and comprehension led to subsequent increases in patient compliance and retention. Medidata Patient Cloud Rave eConsent is our innovative, patient-friendly electronic informed consent and patient enrollment system for clinical trials. This course will cover the new features and enhancements made to Rave Safety Gateway in relation to the 2023. 1 II. Eliminate complex, manual processes & achieve higher quality data for faster insights. CTFM provides Sponsors and CROs with a comprehensive, best-in-class financial. New solutions are needed to minimize adverse impacts to patient enrollment and retention, as well as patient safety and clinical trial integrity. g. Day 3, Wednesday June 22nd. 2. As the industry’s only unified platform dedicated to clinical research, we help life science and medical device organizations cut development costs, mitigate risks, and deliver treatments and devices to market faster. Sep-2019: Signant Health collaborated with the Shanghai Mental Health Centre (SMHC), a leading organization on mental health prevention planning. Built directly on the industry’s leading Rave EDC platform, myMedidata extends all of the capabilities of Medidata’s patient-. Rave Data Management. Certification for the use of Medidata Rave, obtained in 2019, added to our efficiency by elimitating many of the manual steps in the process and improving the delivery time, decision-making process, and real-time. Korean. The evolution in automated medical coding for Rave EDC. Medidata Detect: Using AI Data Reconciliation. The powerful, cutting-edge architecture behind the Medidata Clinical Cloud. Through the use of multimedia. Navigating through the system is a nightmare. Medidata Launch, our twelve week internship program intended for rising seniors and graduate students, allows you to obtain a first-hand understanding of what it means to be a Medidatian. Stitching together different shapes and sources of data, we seek to power new experiences bringing together. The evolution in automated medical coding for Rave EDC. A Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY. TM. Medidata Remote Source Data Review is a cloud-based solution that rapidly and remotely enables monitors to acquire critical documents, automates document workflows to the right monitor for the right study. The Medidata Rave Clinical Cloud is the cutting-edge platform that transforms the clinical trial experience for patients, sponsors, CROs, andMedidata Rave eConsent Dashboard Overview. Rave EDC. Terrible system for end user at the site leads to too many errors and too much money spend correcting them. Real-Time Insights through the Medidata Clinical Cloud • Real-time data visibility into work"ows, study and site performance — report on or extract full trial datasets at any point in the trial • Data captured through any Medidata product (Rave RTSM, Medidata eCOA, Medidata eConsent, Rave Imaging), or an external system connected In a decentralized trial, an electronic consent (eConsent) is used in lieu of traditional paper and wet signatures gathered at a site and enables patients to learn about their studies through an educational video, followed by written details and guidelines. Operationalize your risk management process in a way that spreadsheets. The result is a unified solution that provides a complete picture of your clinical trials’ progress, ensures you are inspection ready, and frees up time and resources so that you can. . “Medidata Rave EDC was the runaway first-choice preference for all trial types – about 40% of respondents deemed Medidata their topMedidata Risk Management provides a dynamic digital solution for risk assessment, monitoring, and mitigation. Leverage our innovative digital technology to enable the shift from 100% on-site monitoring to remote monitoring. Real-Time Insights through the Medidata Clinical Cloud • Real-time data visibility into work"ows, study and site performance — report on or extract full trial datasets at any point in the trial • Data captured through any Medidata product (Rave RTSM, Medidata eCOA, Medidata eConsent, Rave Imaging), or an external system connectedMedidata Rave eConsent A Unified Platform Benefits Patients Reading Time: 3 minutesToday, life science companies and research organizations face unique challenges related to clinical…In a decentralized trial, an electronic consent (eConsent) is used in lieu of traditional paper and wet signatures gathered at a site and enables. Any Rave EDC studies not using eCOA can add eCOA to the project and immediately begin converting forms to remote-enabled forms. Rave EDC. The handling charge (CNY1,230) won’t be subject to refund. Our mission is to put innovative technology and insightful data into your hands, to. Rave Data Management. Email Address. If you have any questions about a course’s content, please feel free to reach out to us at medidata. Rave eConsent Overview for Principal Investigators. Medidata Global Education announces the following New and Updated Materials for October 2023. Companion. Trusted by CROs, sponsors, and sites across all. 2. The Medidata Institute cultivates a thought leadership channel for key players of the life sciences industry to contribute diverse perspectives and redefine how collaborative, cross-sector partnerships can inspire the next generation of healthcare solutions for patients. eConsent. Please contact your Medidata representative for enrollment. eConsent. eLearning courses. View the fact sheet for more information. 9am – 6pm CST (Monday – Friday) Client may request a one-time adjustment to the study Parameters (number of sites, patients, Instruments, devices, countries or translations) for Device Services and/or Other Subscription Services, on or before ninety (90) days from the Sales Order. Medidata Solutions. Rave EDC Is Designed for Clinical Site Users to Succeed. Eliminate complex, manual processes & achieve higher quality data for faster insights. Equip your clinical trial study with fast, accurate medical coding. 25%. APIs vs. Rave Data Management. info@medidata. Title. 13. com eLearnings New courses are now available via iMedidata. Solution. Coder. Rave EDC. Rave EDC. 0 Release Training. Every year, Medidata and its customers perform tens of. Rave EDC. 0 Release Training. The leading unified platform dedicated to clinical research. The study’s 2,726eConsent. 1 Quality risks such as missing documents, wrong documents, missing signatures, missing or wrong dates were also reduced. Medidata Rave eCOA Release Training (R06 2020) Medidata Rave 2020. Leverage Medidata’s automated data anomaly detection system, Centralized Statistical Analytics (CSA), focused on critical safety and. Electronic informed consent technology, such as Medidata Rave eConsent, provides patients with a guided learning experience to gain a better understanding of the study’s purpose, risks, benefits, schedules, and their rights and responsibilities. Over the past year, clinical trials have had to become more modernised because of the strange environment we were operating in. 2. Phase 4. Rave EDC is the cornerstone of the Medidata Clinical Cloud® – the unified clinical research platform that connects processes, eliminates data reconciliation and delivers cross.