Prerequisites
- Medidata Site Monitoring: Visit Management
- Medidata Site Monitoring: Submit, Review, and Approve Visits
- Medidata Site Monitoring: Confirmation and Follow Up Letters
- Getting Started with Medidata Issue Management
Overview
Site Monitoring provides efficient monitoring of clinical studies with integrated workflows to improve the site monitor experience, aid proactive decision making, and reduce risk and costs to ultimately increase study performance, patient safety, and time to market for the drug or device.
This course gives attendees in depth training for the entire end user workflow in Site Monitoring, from planning the site visit all the way through finalizing the follow up letter. Management of issues and action items with Issue Management will also be covered in the course.
Recording of Global Education training sessions is strictly prohibited. Any attempts to record training will result in an immediate stoppage of training until recording is terminated.
Course Type
Instructor-led Classroom, Instructor-led Web-based
Audience
Monitors, Project Managers (Clinical)
Max Attendees
20
Duration
Remote offering is 2 half day sessions.
Instructor Led Classroom style is 1 day.
Languages
Chinese (Simplified), English, Japanese, Korean
Product
Medidata Site Monitoring
Training Units
1
Cancellation
Please review the Medidata Academy Training Delivery Cancellation Policy prior to scheduling.