Rave CSA Critical Fundamental
All clinical research stakeholders are navigating a “new normal,” due to the COVID-19 pandemic that requires agile adaptation of technology, processes, and resources for current and future research efforts. This paradigm shift necessitates patients, sites, CROs, and sponsors to rapidly come up with novel, creative solutions to minimize adverse impacts to patient safety and clinical trial integrity. Medidata is here to help during this time by providing centralized data ingestion, integration, and analysis with Rave CSA Critical - a solution that mitigates your limited resources. Central monitoring can be used to rapidly assess which studies have been impacted by COVID-19 and to what extent. This Rave CSA Critical package should be used alongside study-specific risk assessment and mitigation strategies.
In this eLearning, you will learn about the basics of the Rave CSA Critical offering. Topics include:
CSA Critical Overview
CSA Critical Navigation
Biostatisticians, Clinical Trial Administrators, Data Managers, Global Trial Managers, Monitors, Project Managers (Clinical), Site/User Administrators, Statisticians
Rave CSA Critical Fundamental - eLearning Outline - ENG