TY  - BOOK
AU  - Tranquillo,Joseph,Vincent
AU  - Goldberg,Jay R.
AU  - Allen,Robert
TI  - Biomedical engineering design
T2  - Biomedical engineering
SN  - 9780128164440
AV  - R856 .T72 2023
PY  - 2023///
CY  - London
PB  - Elsevier
KW  - Biomedical engineering
KW  - Technological innovations
KW  - Medical instruments and apparatus
KW  - Design and construction
KW  - Génie biomédical
KW  - Innovations
KW  - biomedical engineering
KW  - aat
KW  - fast
N1  - Contents:
1. Introduction--
2. Design Teams and Project Management--
3. Defining the Medical Problem--
4. Defining the Engineering Problem--
5. Generating Solution Concepts and Preliminary Designs--
6. Selecting a Solution Concept--
7. Prototyping--
8. Detailed Design--
9. Testing for Design Verification and Validation--
10. Testing in Living Systems--
11. Medical Device Standards and Design Controls--
12. Regulatory Requirements--
13. Ethics in Medical Device Design--
14. Beyond Design: The Engineer's Role in Design Transfer, Commercialization, and Post Market Surveillance--
15. Collaborating on Multifunctional Teams to Commercialize Medical Products
N2  - Biomedical Engineering Design presents the design processes and practices used in academic and industry medical device design projects. The first two chapters are an overview of the design process, project management and working on technical teams. Further chapters follow the general order of a design sequence in biomedical engineering, from problem identification to validation and verification testing. The first seven chapters, or parts of them, can be used for first-year and sophomore design classes. The next six chapters are primarily for upper-level students and include in-depth discussions of detailed design, testing, standards, regulatory requirements and ethics. The last two chapters summarize the various activities that industry engineers might be involved in to commercialize a medical device

ER  -