Monitorering
Course in monitoring in clinical studies, with a focus on quality assurance and follow‑up during study conduct.
Intro
Course in monitoring in clinical studies, with a focus on quality assurance and follow‑up during study conduct.
Target group
The course is intended for research nurses, nurses and other staff who work with or plan to work with monitoring in clinical studies or investigator‑initiated trials.
Course overview
The course provides a basic understanding of monitoring, why it is needed and how it is performed in practice.
Prerequisites
Participants should have at least one year of experience working with clinical trials, or have completed a basic course in clinical trials or equivalent.Basic knowledge of GCP is recommended. Previous experience of monitoring is not required.
Course content
- Taking on a monitor role
- Monitoring plan
- Trial Master File (TMF)
- Study start‑up and initiation visit
- Monitoring visits – preparation and conduct
- Study close‑out
- Audits and inspections
- Writing monitoring reports
- Practical monitoring exercises
- Review and discussion
Practical information
Language
The course is delivered in Swedish and concludes with a certificate
Location
Uppsala (UCR or Uppsala University Hospital premises)
Exact location will be communicated approximately two weeks before the course starts
Course dates
Upcoming course dates are listed below
Fees
SEK 5,300 (excluding VAT)
Lunch, refreshments and course materials are included
Cancellation policy
Cancellations can be made free of charge up to 14 days before the course starts
Later cancellations will be charged according to the course terms