42060 Biomedical Industry Frameworks
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Subject handbook information prior to 2020 is available in the Archives.
Credit points: 6 cp
Subject level:
Postgraduate
Result type: Grade and marksDescription
This subject introduces students to the various frameworks, procedures and regulations that are commonplace within the biotech/medical device industry. Students learn to identify standard mechanisms associated with quality systems, regulatory affairs, design processes and risk analyses essential to operating within the industry. Further, they gain skills to apply the relevant tools within each of these areas. Students gain an understanding of regulatory environments both within Australia and overseas. This subject provides a foundation for students to enter the regulated environment of biotech businesses and to operate from an informed position within them.
Subject learning objectives (SLOs)
Upon successful completion of this subject students should be able to:
| 1. | Analyse the biomedical industry regulations to understand the various aspects of health-related systems and products. |
|---|---|
| 2. | Identify standard mechanisms associated with quality systems. |
| 3. | Evaluate regulatory affairs, design processes and risk analysis. |
| 4. | Analyse regulatory environments both within Australia and overseas. |
| 5. | Present findings to a variety of audiences including stakeholders. |
Course intended learning outcomes (CILOs)
This subject also contributes specifically to the development of the following Course Intended Learning Outcomes (CILOs):
- Socially Responsible: FEIT graduates identify, engage, and influence stakeholders, and apply expert judgment establishing and managing constraints, conflicts and uncertainties within a hazards and risk framework to define system requirements and interactivity. (B.1)
- Technically Proficient: FEIT graduates apply theoretical, conceptual, software and physical tools and advanced discipline knowledge to research, evaluate and predict future performance of systems characterised by complexity. (D.1)
- Collaborative and Communicative: FEIT graduates work as an effective member or leader of diverse teams, communicating effectively and operating autonomously within cross-disciplinary and cross-cultural contexts in the workplace. (E.1)
Teaching and learning strategies
Workshop class sessions including interactive class discussions and collaborative activities.
Readings on core topics and assignments.
Case studies.
Students will be able to work in teams and will receive feedback about the progress of their work. Summative and informative feedback will be provided for each assessment task.
Content (topics)
- Industry Overview – regulated industries, local & international biotech industry, product types and latest innovations, industry trends
- The Design & Development Process – phases of the process, their purpose and intent
- Regulatory Affairs & its role in the business – regional bodies, essential principles, requirements for products, gaining approval
- Quality Management Systems (QMS) – standards, device control files, quality systems, customer facing systems
- Risk Management – definition and importance, standard tools, adverse events
- Intellectual Property (IP) – importance, considerations, patents
- Ethics – clinical trials, animal testing, gaining customer feedback
Assessment
Assessment task 1: Pitch
| Intent: | Students to pitch their topic for the project – provides the opportunity to consider the customer needs first rather than the technology solution. Pitching a new MedTech idea, concisely. Defining a MedTech market need, customer, and conducting initial market research. |
|---|---|
| Objective(s): | This assessment task addresses the following subject learning objectives (SLOs): 5 This assessment task contributes to the development of the following Course Intended Learning Outcomes (CILOs): E.1 |
| Type: | Presentation |
| Groupwork: | Group, group assessed |
| Weight: | 5% |
| Length: | Time limit = 4 minutes (+ 1-minute Q&A) |
Assessment task 2: Design for User Case Study
| Intent: | Provides specific case study of “design for user” in medical device technology. |
|---|---|
| Objective(s): | This assessment task addresses the following subject learning objectives (SLOs): 2, 3 and 4 This assessment task contributes to the development of the following Course Intended Learning Outcomes (CILOs): B.1 and D.1 |
| Type: | Case study |
| Groupwork: | Individual |
| Weight: | 40% |
Assessment task 3: Final presentation
| Intent: | Provides a complete end-to-end MedTech device development portfolio, from conception of the idea to implementation to market. Group presentation of group work and findings. |
|---|---|
| Objective(s): | This assessment task addresses the following subject learning objectives (SLOs): 1, 2, 4 and 5 This assessment task contributes to the development of the following Course Intended Learning Outcomes (CILOs): B.1, D.1 and E.1 |
| Type: | Presentation |
| Groupwork: | Group, group assessed |
| Weight: | 15% |
| Length: | Time limit = 8 minutes (+ Q&A) |
Assessment task 4: Final report
| Intent: | Provides a complete end-to-end MedTech device development portfolio, from conception of idea to implementation to market. Individual report is based on group-project topic. To provide an overview of the end-to-end process required to deliver a new MedTech device to market. |
|---|---|
| Objective(s): | This assessment task addresses the following subject learning objectives (SLOs): 1, 2, 3 and 4 This assessment task contributes to the development of the following Course Intended Learning Outcomes (CILOs): B.1 and D.1 |
| Type: | Report |
| Groupwork: | Individual |
| Weight: | 40% |
| Length: | 15 page limit, including FMEA (plus references & cover sheet). |
Minimum requirements
In order to pass the subject, a student must achieve an overall mark of 50% or more.