Work-based content
Competencies
# | Learning outcome | Competency | Action |
---|---|---|---|
# 1 | Learning outcome 1,2 |
Competency
Implement interdisciplinary medical device risk management forums within the institution |
Action View |
# 2 | Learning outcome 3 |
Competency
Undertake medical device audits |
Action View |
# 3 | Learning outcome 6 |
Competency
Provide advice on the requirements for a clinical trial involving a novel medical device |
Action View |
# 4 | Learning outcome 4,5 |
Competency
Keep up to date with new technologies and developments within the field of medical device management |
Action View |
# 5 | Learning outcome 4,5 |
Competency
Advise the institution on equipment replacement requirements |
Action View |
# 6 | Learning outcome 4 |
Competency
Participate in the clinical engineering response to a major business plan involving a significant medical equipment installation |
Action View |
Assessments
You must complete:
- 1 case-based discussion(s)
- 1 of the following DOPS/ OCEs:
Underake an audit of medical device use in clinical practice | DOPS |
Assess the impact of emerging regulation or standardisation | DOPS |
Use engineering principles to determine the best engineering solutions to effectively manage medical devices | DOPS |
Contribute to interdisciplinary forum to promote the safe and effective use of technology e.g. Medical Device Advisory Groups | OCE |
Present recommendations to a multi disciplinary group on achieving compliance with a medical device guideline | OCE |
Learning outcomes
- Establish and run interdisciplinary forums to promote the safe and effective use of technology, eg medical device advisory groups
- Serve as a contributing member of appropriate committees as required, eg equipment committees, governance or audit forums
- Audit medical device issues as requested
- Provide strategic business advice to the institution, eg medical device equipment replacement forecasts
- Assess the impact of emerging regulation or standardisation
- Advise on ad-hoc technical issues