u003ch1 class=u0022h-lgu0022u003eMedidata EDC Bundle Webinarsu003c/h1u003e
u003cp class=u0022h-lg t-bodyu0022u003eu003cstrongu003eUnderstanding more about Detect, Companion and Medidata Patient Cloudu003c/strongu003eu003c/pu003e
u003cspan style=u0022font-weight: 400;u0022u003eMedidata’s Rave EDC (Electronic Data Capture) is the most advanced, robust, and secure EDC system for clinical trial site, patient, and lab data capture and management. u003c/spanu003e
u003cspan style=u0022font-weight: 400;u0022u003eRave EDC is the cornerstone of the u003c/spanu003eu003ca href=u0022https://www.medidata.com/en/clinical-trial-products/unified-platformu0022u003eu003cspan style=u0022font-weight: 400;u0022u003eMedidatau003c/spanu003e Platformu003c/au003eu003csupu003e u003c/supu003eu003cspan style=u0022font-weight: 400;u0022u003e- the unified clinical research platform that connects processes, eliminates data reconciliation, and delivers cross-functional and cross-study data insights.u003c/spanu003e
u003cstrongu003eWatch the following webinars on-demand to learn more about how EDC works with the various solutions in Medidata. u003c/strongu003e
Find out more about Medidata Detect
To improve the quality and efficiency of clinical trials, regulatory agencies have developed several approaches, including Quality by Design and Risk-Based Quality Management (RBQM).
In this webinar, we will discuss about quality build into clinical trial design from the beginning u0026amp; emphasize on ICH E8(R1) guidelines. How does centralized statistical monitoring solves many challenges in a comprehensive data surveillance and risk management solution that allows cross-functional teams to monitor and mitigate risks to data integrity and patient safety.
Find out more about Medidata Companion
One of the most resource-intensive, mundane, yet essential tasks in a clinical trial is the manual process of patient data entry. It usually includes transcription and validation of source data from an EHR or an eCRF into an EDC.
The easiest way to avoid errors at entry, while at the same time accurately feeding patient data to the EDC system, is to streamline the data directly from the Electronic Healthcare Records (EHRs) to EDC forms. Direct data sourcing from EHRs is a challenging task that only fully integrated clinical trial software solutions can achieve. In general, it can be accomplished by interoperability.
In this presentation we would like to discuss tool streamlines and expedites clinical trial data entry by extracting data from Electronic Health Records (EHR) and other systems into Rave EDC. This saves time for trial sites, allowing them to focus more on patient care. The integration reduces errors and improves data quality.
Find out more about Medidata Unified Platform Approach
“Metadata” is an essential part of any application. In an integrated model, there are different data sources used to drive the same type of data across different applications. The unified platform creates a single data source and reporting solution, which inspires self-service through one common login, drives efficiency, simplifies training, and enables users to build and deploy their reports—all at a lower cost.
Most importantly in medical research time is money. Patient, site-staff, investigator, or sponsor – all users benefit from an intuitive experience and orchestrated workflows.
In this webinar we will discuss how to leverage on unified platform and achieve patient centric, site centric and oversights for sponsors approaches.