Medical Devices Course Schedule

 This chart outlines the program curriculum and annual schedule. Click here to read course details and enroll.
  ■ = classroom   O = online   ▲ = hybrid
☐ = both online and classroom sections available
Courses Units Course Fall Winter Spring Summer
Design Control for Product Development 2.0 21973 ■

Electronic Records for Regulated Environments: Cost-Effective Approaches to Compliance 1.5 19362 ■
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Global Medical Device Submissions and Strategy 1.5 20343
   
Human Factors in Medical Device Development 2.0 23097  
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Human Physiology in Health and Disease 3.0 6999 ■ ■    
Intellectual Property Essentials for the Life Science Industry 1.0 1942     ■
Medical Device Design and Development 2.0 19977 ■   ■  
Medical Devices: Regulatory Strategies and Marketing Pathways 1.5 5939   ■  
Molecular Diagnostics 1.5 21972
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Nanotechnology, Introduction 1.0 4820  
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Post-Market Regulatory Obligations for Medical Devices 1.5 22414
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Product Development Life Cycle for Medical Devices 2.0 23084



Regulation of Biomedical Product Advertising, Promotion and Labeling 1.5 20756
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Regulation of Medical Devices and Diagnostics 3.0 19071   ■  
Regulatory Compliance for Medical Devices 2.5 19029 ■   ■  
Regulatory Submissions: Devices and Diagnostics 2.5 19315   ■   ■
Risk Management for Regulated Industries 3.0 22631   ■   ■
Statistical Design of Experiments: A Practical Approach 2.0 23096  
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Value-Added Quality Audits 1.5 19073       ■

 

Free Events Units Course Fall Winter Spring Summer
Biosciences Program Presentation: Biotechnology, Bioinformatics and Bioscience Business   16649
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Clinical Trials and Regulatory Affairs 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.