Online Clinical Research, Clinical Trials and Ethics Courses

PRAXIS Australia is a leading Australian and International NFP education and training provider. Our training offers are built upon the competencies developed by the Harvard Multi-Regional Trials Centre (MRCT) and aligned to competencies recommended by the NHMRC.

These training offers are regarded as a benchmark for researchers, clinical trials, and healthcare professionals in Australia and internationally.

PRAXIS maintains course content to ensure all information is current. Our GCP courses are up-to-date with current ICH regulations E6 (R2).

Further updates to GCP, E6 (R3) are anticipated to be confirmed in late 2025/2026.

PRAXIS will be updating course content when the changes are made.

Research Essentials

Our world class research training program, designed for Research Investigators, Coordinators, Managers and Assistants. Build your own study plan from a selection of over 65 unique modules and electives.

HREC Essentials

Australia’s only accredited training course for Human Research Ethics Committees. Provides committee members with a deeper understanding of the purpose and function of HRECs.

Core Skill Sets

Adopting a learner-centred approach, our Core Skill Sets empower you to create your own customised study plan composed of 8 modules and 2 electives of your choice.

HREC for Busy People

A training solution for those who need to upskill but don’t have the time or resources. This course will provide you with the fundamental knowledge needed to work in ethics and governance.

Research with Aboriginal and Torres Strait Islander Peoples online module

This module will explore ways to help you make decisions to ensure the research journey benefits and respects Aboriginal and Torres Strait Islander people and communities, their rights, culture, heritage, land and resources.

Good Clinical Practice online module

This TransCelerate endorsed, fully online module will introduce you to the internationally recognised and endorsed Good Clinical Practice standards (E6 R3) and the roles and responsibilities of all those involved in conducting research involving humans.

New GCP for Medical Devices | ISO 14155:2026 | Updated Courses

If your team is involved in medical device research, clinical trials, ethics review, governance, sponsorship, development or commercialisation, this updated online training pathway will help strengthen your understanding of device-specific GCP and ISO 14155:2026.

Suggestion box: new offers and interest areas

What would you like to see from us? This can be a topic we haven't covered yet, a course style, or a different way of delivering our courses and workshops. All suggestions are welcome and will be considered.

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