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“Very useful knowledge for the changes that are coming in Australia regarding the conduct of clinical trials [in 2023-24].”

"I’ve attended quite a few PRAXIS workshops now. The content across the workshops I’ve attended has always been presented in clear and accessible ways, and I always come away with a sense of how I can utilise that information in my role."

"The whole [HREC] course was extremely valuable and provided a lot of useful information and perspectives that certainly helped to broaden my understanding of the role of HRECs."

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 is successfully building the confidence, competence and capability of the clinical trials, medtech, research and ethics sectors.  We are achieving this by collaborating with government, industry, academia and advocacy organisations across the sector.

PRAXIS has been contracted to develop training on behalf of the Australian Commission on Safety and Quality in Health Care. This training will be delivered by the Commission to assessors who will be reviewing Australian clinical trial sites against the Framework from 2023. In alignment with the training materials we’ve developed for the Commission, we are happy to support you and your team with training solutions to help you prepare for these requirements.

7 December 2023, 10.00am – 2.00pm

Better navigate privacy law and regulations to avoid common privacy risks in your research. You’ll get to learn about unique challenges and strategies for success.

1 February 2024, 10.00am – 2.00pm

This virtual workshop will provide you with the skills and confidence you need to successfully Chair a Committee.

7 February 2024, 10.00am – 2.00pm

Suitable for those working across the development lifecycle of Medical Devices including regulators, industry, researchers, research site staff and HREC and governance.

Thursday, 15 February 2024, 10.00am – 2.00pm

Explore techniques to amplify the voices of consumers while fostering a collaborative environment that drives meaningful impact.

Tuesday, 20 February, 10.00am – 2.00pm

Gain an overview of the scientific, ethical and practical issues involved in the design and conduct of paediatric research.

29 February 2024, 10.00am – 2.00pm

Gain expert guidance on your Standard Operating Procedure (SOP) development, and how to align your SOPs to quality management principles and standards.

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