Module Details
Module Code: |
BIOE7004 |
Title: |
Biomedical Manufacture
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Long Title:
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Biomedical Manufacture
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NFQ Level: |
Intermediate |
Valid From: |
Semester 1 - 2016/17 ( September 2016 ) |
Field of Study: |
5212 - Biomedical Engineering
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Module Description: |
This module has been designed to introduce the student to the processes and work practices that are employed in the manufacture of medical devices.
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Learning Outcomes |
On successful completion of this module the learner will be able to: |
# |
Learning Outcome Description |
LO1 |
Describe the specifications and requirements for cleanrooms in the medical device industry |
LO2 |
Describe the appropriate cleaning, packaging and sterilisation operations for medical devices |
LO3 |
Explain the safety risks associated with a manufacturing operation and understand the requirements for guaranteeing a safe working environment. |
LO4 |
Identify the requirements of a GMP system and explain the operation of regulatory bodies such as FDA/IMB. |
LO5 |
Explain the validation requiments for medical device design and manufacture. |
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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Not applicable |
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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Not applicable |
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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Not applicable |
Indicative Content |
Cleanroom Technology
Cleanroom classification; particle size and counting; filter design and performance, cleanroom layout, materials & standards.
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Cleaning and Sterilisation Technology
Requirements for cleaning, soil types, cleaning systems organic/aqueous /semiaqueous), cleaning equipment. Ethylene oxide. Gamma sterilisation, electron beam. Saturated steam - gravity displacement, porous load, ballasted cycles. Dry heat sterilisation/depyrogenation. Microbial inactivation/endotoxin inactivation.
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Packaging
Functions of packaging, packaging requirements for sterilisation, physical properties of packaging, labelling and packaging control, distribution hazards, production of packages, forming materials and methods, lidding, sealing.
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Machine Safety
Risk assessment, use of machines, identifying the hazards, machine situations giving rise to risk
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GMP
Introduction to GMP, GMP documentation - SOPs/regulatory documentation/submissions, Role and requirements of the FDA/IMB/Notified Bodies, introduction to 21 CFR820/Medical Devices Directive, planning for audits.
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Validation
Validation protocols - Installation, operational and performance qualification. Process validation, design Qualification, validation of sterilisation system, design verification, design validation.
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Module Content & Assessment
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Assessment Breakdown | % |
Coursework | 20.00% |
End of Module Formal Examination | 80.00% |
Assessments
End of Module Formal Examination |
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Reassessment Requirement |
Repeat examination
Reassessment of this module will consist of a repeat examination. It is possible that there will also be a requirement to be reassessed in a coursework element.
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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 |
Class based instruction |
Every Week |
4.00 |
4 |
Independent & Directed Learning (Non-contact) |
Non Contact |
Self directed learning to complement lecture material |
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 |
Class based instruction |
Every Week |
3.00 |
3 |
Independent & Directed Learning (Non-contact) |
Non Contact |
Self directed learning to complement lecture material |
Every Week |
4.00 |
4 |
Total Hours |
7.00 |
Total Weekly Learner Workload |
7.00 |
Total Weekly Contact Hours |
3.00 |
Module Resources
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Recommended Book Resources |
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Lerouge, Sophie and Simmons, Anne. (2012), Sterilisation of Biomaterials and Medical Devices, 1. Woodhead Publishing, [ISBN: 9781845699321].
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W. Whyte. (2010), Cleanroom Technology, John Wiley & Sons, Chichester, West Sussex, U.K., [ISBN: 9780470748060].
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edited by Max Sherman. (1998), Medical device packaging handbook, Marcel Dekker, New York, [ISBN: 0824701992].
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Itay Abuhav,. (2011), ISO 13485: A Complete Guide to Quality Management in the Medical Device Industry, 1st. CRC Press, [ISBN: 9781439866115].
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edited by John Ridley and John Channing. (2003), Safety at work, Butterworth Heinemann, Oxford [England], [ISBN: 0750654937].
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edited by Stephen P. Denyer, Rosamund M. Baird. (2006), Guide to microbiological control in pharmaceuticals and medical devices, CRC Press, Boca Raton, Fla., [ISBN: 9780748406159].
| Supplementary Book Resources |
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Joseph F. Hanlon, Robert J. Kelsey, Hallie E. Forcinio. (1998), Handbook of package engineering, Technomic Pub. Co., Lancaster, Pa., [ISBN: 9781566763066].
| This module does not have any article/paper resources |
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Other Resources |
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Website, Food and Drug Administration. FDA Website,
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Website, European Commission. (1993), European Commission Website,
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