Module Details
Module Code: |
BIOE8009 |
Title: |
Health Technology Management
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Long Title:
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Health Technology Management
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NFQ Level: |
Advanced |
Valid From: |
Semester 2 - 2022/23 ( January 2023 ) |
Field of Study: |
5212 - Biomedical Engineering
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Module Description: |
The learners are presented with real and authentic scenarios, case studies or other ill-structured problems. The learners will explore various aspects of a Clinical Engineering Management Plan including stakeholders analysis, models of management, standards, safety and resource constraints to solve and communicate the sociotechnical challenges in the management of the Clinical Engineering Department and Healthcare Technology.
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Learning Outcomes |
On successful completion of this module the learner will be able to: |
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Learning Outcome Description |
LO1 |
Create using best practice and supported by group engagement, a health technology management plan from a systems engineering theory perspective as applied to a clinical setting. |
LO2 |
Formulate a non-vendor specific technical specification for health technology from patient and clinical user requirements informed by WHO guidance documents. |
LO3 |
Analyse Clinical Engineering's role in the delivery of quality healthcare through healthcare technology management, economic models, data protection, patient safety and risk. |
LO4 |
Evaluate the socio-technical challenges of solving Clinical Engineering problems such as healthcare technology management, safety, information technology, facilities management and human resources. |
Dependencies |
Module Recommendations
This is prior learning (or a practical skill) that is strongly recommended before enrolment in this module. You may enrol in this module if you have not acquired the recommended learning but you will have considerable difficulty in passing (i.e. achieving the learning outcomes of) the module. While the prior learning is expressed as named MTU module(s) it also allows for learning (in another module or modules) which is equivalent to the learning specified in the named module(s).
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Incompatible Modules
These are modules which have learning outcomes that are too similar to the learning outcomes of this module. You may not earn additional credit for the same learning and therefore you may not enrol in this module if you have successfully completed any modules in the incompatible list.
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No incompatible modules listed |
Co-requisite Modules
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No Co-requisite modules listed |
Requirements
This is prior learning (or a practical skill) that is mandatory before enrolment in this module is allowed. You may not enrol on this module if you have not acquired the learning specified in this section.
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No requirements listed |
Indicative Content |
Health Technology Management
Stakeholders analysis, Clinical Engineering support of medical devices throughout the device life cycle. Maintenance requirements of medical device technologies. Techniques to evaluate the most economical method in maintaining medical device technologies. Sourcing standards required in medical device management. Resources required in medical device management. Safeguarding the organisation's investment. CE alignment with the Six Aims of Quality Healthcare. Systems engineering theory as applied to the clinical setting. Project Management principles as applied to clinical engineering, medical technology life cycle.
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Medical Device Technical Specification
Requirements Elicitation, determination and analysis of sources of information on medical device technologies. The EU process for technical specifications and rules. How and why medical device standards are formulated, World Health Organisation (WHO) health technology specifications. EU tendering laws. Design techniques in evaluation of medical device technologies.
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Minimising Clinical Risk in Management of Medical Devices
Medical error, human error for medical devices. IEC 62366-1:2015 usability. Clinical risk in the management of medical device technologies. Design and evaluation of systems to minimise risk in the use of medical technologies. Understanding and interfacing with regulatory bodies in the reporting and dissemination of medical device incidents. Design of methodologies to evaluate medical device companies/distributors to ensure proper systems are in place in the event of a medical device incident.
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Information Communication Technology
The human-device interface and human factors, computerized maintenance management systems, medical device interoperability and integration, cybersecurity, threats, and patient data, data driven decisions and data analytic techniques, emerging technologies and technology transfer into healthcare settings.
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Facilities Management
Peripheral and support service requirements for medical devices in the clinical, community and homecare settings, clinical rooms requirements, emergency preparedness, infection prevention and control.
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Human Resource Management
Culture of safety, continuous professional development, biomedical/clinical engineering vendor/technology specific training requirements and record management, change management. Certification of Clinical Engineering in Ireland and internationally.
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Module Content & Assessment
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Assessment Breakdown | % |
Coursework | 100.00% |
Assessments
No End of Module Formal Examination |
Reassessment Requirement |
Coursework Only
This module is reassessed solely on the basis of re-submitted coursework. There is no repeat written examination.
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The University reserves the right to alter the nature and timings of assessment
Module Workload
Workload: Full Time |
Workload Type |
Contact Type |
Workload Description |
Frequency |
Average Weekly Learner Workload |
Hours |
Lecture |
Contact |
Lectures and discussions to address the learning outcomes and indicative content |
Every Week |
4.00 |
4 |
Independent Learning |
Non Contact |
Engaging with the learning outcomes and reflecting and contributing to the group work activity |
Every Week |
3.00 |
3 |
Total Hours |
7.00 |
Total Weekly Learner Workload |
7.00 |
Total Weekly Contact Hours |
4.00 |
Workload: Part Time |
Workload Type |
Contact Type |
Workload Description |
Frequency |
Average Weekly Learner Workload |
Hours |
Lecture |
Contact |
Lectures and discussions to address the learning outcomes and indicative content |
Every Week |
4.00 |
4 |
Independent Learning |
Non Contact |
Engaging with the learning outcomes and reflecting and contributing to the group work activity |
Every Week |
3.00 |
3 |
Total Hours |
7.00 |
Total Weekly Learner Workload |
7.00 |
Total Weekly Contact Hours |
4.00 |
Module Resources
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Recommended Book Resources |
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Roberto Miniati, Ernesto Iadanza, and Fabrizio DORI. (2016), Clinical Engineering : From Devices to Systems, Elsevier Science & Technology, [ISBN: 9780128038246].
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Samantha Jacques, PhD, FACHE and Barbara Christe PHD. (2020), Introduction to Clinical Engineering, 1st. Elsevier Academic Press, [ISBN: 9780128181034].
| Supplementary Book Resources |
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Dyro, Joseph F. (2004), Clinical Engineering Handbook, Elsevier Academic Press, [ISBN: 012226570X].
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Institute of Medicine. (2000), To Err is Human: Building a Safer Health System, [ISBN: 9780309068376].
| This module does not have any article/paper resources |
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Other Resources |
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Website, World Health Organisation,
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Website, Food and Drug Administration,
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Website, European Medicines Agency,
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Website, European Network for Health Technology
Assessment,
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Website, Biomedical Engineering Associatin of
Ireland,
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Website, American College of Clinical Engineers,
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Website, American Society for Health Care
Engineering,
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