Overview
Offerings
Requisites
Rules
Contacts
Chief Examiner(s)
Unit Coordinator(s)
Learning outcomes
Analyse and assess the regulatory frameworks, human ethics and sustainable practices that guide the production of medical devices to justify different paths to market approval.
Generate plans for conceptual designs of new medical technology devices that identify gaps and opportunities to make an impact in the health industry.
Prioritise responses to feedback from patient and health professional stakeholders through the proposal of new hypothetical but feasible medical technology devices after reflection and synthesis of collected knowledge.
Research and synthesise knowledge gathered from Australian and international medtech business cases to develop a business plan, taking into consideration manufacturing, technical and financial feasibility.
Demonstrate effective collaboration as a team member by participating in all group activities and conducting regular self- and peer-assessment of individual and team performance.
Assessment summary
Continuous assessment: 70%
Final assessment: 30%
This unit contains hurdle requirements that you must achieve to be able to pass the unit. You are required to achieve at least 45% in the total continuous assessment component and at least 45% in the final assessment component. The consequence of not achieving a hurdle requirement is a fail grade (NH) and a maximum mark of 45 for the unit.
The assessments of this unit are designed to demonstrate the achievement of the advanced learning outcomes and standards expected of Master’s level coursework.