Skills for Monitoring Non-Commercial Clinical Trials (UK)

Registration is now open for the following courses"

• October 26-27, London — Register
• December 6-7, Manchester — Register

Course Description
A Training Course for Monitoring Clinical Trials of Medicinal Products in the Non-Commercial Sector
This two-day course will provide an introduction to the skills required for monitoring research in the UK non-commercial sector. The course will focus on monitoring of clinical research trials of medicinal products. The course is designed for all staff involved in monitoring, or supervising monitoring of clinical research e.g.  R&D Managers, research governance staff, study coordinators, and investigator site staff.

This course is run by ACRP in collaboration with the National Health Service R&D Forum.

Learning Objectives
Upon successful completion of this course, participants should be able to:

• Define the purpose and scope of monitoring
• Understand the responsibilities of individuals associated with monitoring activities
• Identify the monitoring tasks required during the life cycle of a research study
• Monitor adherence to the Principles of Good Clinical Practice and UK regulations of clinical research
• Perform essential skills required for monitors
• Write effective monitoring reports and identify the follow up actions

Agenda
Download the course agenda (.pdf).

Cost
Costs £425 per person for the two-day course. 

Contact
If you interested in hosting the event to save travel and accommodation costs please contact siobhan@acrpnet.org for further details.
For further information on the course and to provisionally reserve a place on future training dates when they are released please contact:

Siobhan Lim, RN, BSc, CCRC
Manager Clinical Research Training, ACRP
European Office, Windsor
Email: siobhan@acrpnet.org    
Tel: 00 44 1753 831 908