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 covers the workflow for confirmation and follow up letters during site visits. Topics include:
- Editing and Finalizing Confirmation Letters
- Editing and Finalizing Follow Up Letters
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
eLearning
Audience
Clinical Operations, Clinical Trial Administrators, Data Entry Personnel, Monitors
Duration
8 min
Languages
English
Product
Medidata Site Monitoring
Course Supplements
eLearning Outline - Medidata Site Monitoring: Confirmation and Follow Up Letters (ENG)