eResearch: Managing Clinical Trials in an Electronic Environment
More and more companies are going “paperless.” What does this mean in the field of clinical research?
This training program examines the challenges of working with electronic documents and how to overcome them. Learn how to set up and manage electronic clinical research documents in compliance with U.S. and EU regulations, and current trends from both the site and sponsor perspectives.
Job aids in the form of compliance checklists (CDISC user requirements and site-level electronic records compliance) and website references are included to ensure you achieve compliance in a paperless clinical trial environment.
Upon completion of this training program, participants should be able to:
Apply regulations and guidance related to the management and use of electronic tools in clinical research.
Evaluate the use of electronic tools and electronic medical records (EMRs) by sites and sponsors during clinical trials.
Employ “best practices” for the completion and monitoring of electronic case report forms (eCRFs) and electronic informed consent forms (eICFs) based on multiple electronic source documents.
This course helps clinical researchers of all types build competency in Clinical Trials Operations (GCPs), Data Management and Informatics, and Study and Site Management. Explore Competencies >