Medical Devices Course Schedule

This chart outlines the certificate curriculum (pending academic approval, excepted for the summer 2012). Click here to read course details and enroll.
  ■ = classroom   O = online   ▲ = hybrid
☐ = both online and classroom sections available
Required Courses Units Course Fall Winter Spring Summer
Introduction to Medical Device Regulation 1.5 30058 ■ ■    
Medical Device Quality Systems 2.5 30087 ■   ■  
Design Control for Medical Devices
 2.0 21973 ■


Risk Management for Regulated Industries 3.0 22631   ■   ■
Human Factors and Usability in Medical Device Development 2.0 23097  
 ■   ■

 

  ■ = classroom   O = online   ▲ = hybrid
☐ = both online and classroom sections available
Elective Courses Units Course Fall Winter Spring Summer
Mobile Medical Applications 0.5 30045   ■   ■
Medical Device Verification and Validation 1.5 30042 ■      
Product Development Life Cycle for Medical Devices 2.0 23084



Post-Market Regulatory Obligations for Medical Devices 1.5 22414
  ■
  
Electronic Records for Regulated Environments: Cost-Effective Approaches to Compliance 1.5 19362 ■
   ■  
Regulation of Biomedical Product Advertising, Promotion and Labeling 1.5 20756 ■    
Value-Added Quality Audits 1.5 19073       ■

 

Free Events Units Course Fall Winter Spring Summer
Clinical Trials, Regulatory Affairs, and Medical Devices Program Presentation   16650
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Note: Individual courses may be taken without enrolling in the full certificate. Course schedule is subject to change, but reflects the current quarter and the anticipated schedule for the next three quarters. Check individual course descriptions for the latest scheduling information.