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The design process required to produce biomedical devices, research equipment, and clinical tools is developed. Topics include identification of need; requirements specification; project management; working in teams; solutions conceptualization, refinement, and selection; hazard and risk analysis and mitigation; verification; validation; regulatory requirements; and medical device pathways to the market. Through critical examination of contemporary medical research and clinical problems, students, working in teams, will identify a need to develop a specific problem statement, project plan, input requirements, solution concept and risk analysis. Recommended preparation: EBME 310.
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| Credits: |
2 |
| Dates: |
May 13 - May 31 |
| Times: |
MTWRF 9:30 a.m.-12:00 p.m. |
| Instructor: |
Dustin Tyler |
| Contact: |
dustin.tyler@case.edu |
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