Monitoring Approved Research: Understanding how to manage research risk across your organisation

This workshop will consider local regulatory requirements and guidance related to monitoring of ethically approved research and clinical trials.

It will allow students to better understand the role, purpose and function of monitoring in clinical research, and the role and responsibility of the institution and HREC, and other key stakeholders Through discussion and case scenarios, we will explore expectations and requirements including researchers and research support staff.


$550 plus GST

Discounts apply for group bookings of 10 or more.

Dates & Locations

Given the impacts of COVID19, new dates and locations will be released as travel restrictions ease around the country. Subscribe to our news to be informed of new dates and location as they are released.

We can also conduct this session at your location for groups of 10 or more. Ask us about this today.

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