Details

ASQ offers enhanced education to individuals preparing for certification and job enhancement by providing a wide range of classes in biomedical and regulatory affairs.

Courses and Classes
Course Title Sub-Title Location
B104 Software Risk Assessment, Verification and Validation for Regulated Industries Software Risk Assessment, Verification and Validation for Regulated Industries Corporate Inn Sunnyvale
B108 - Managing Corrective Actions and Preventive Actions (CAPA), Nonconforming Materials Reports (NCMR) and Deviations CAPA, NCMR and Deviations Corporate Inn Sunnyvale
B101 Introduction to the Biomedical Industry Intro to the Biomedical Industry Corporate Inn Sunnyvale
B102 Quality System Regulation for Medical Devices QSR Corporate Inn Sunnyvale
B103 Preparing & Submitting 510K & PMA Submissions 510K & PMA Submissions Corporate Inn Sunnyvale
B105 Process Validation Process Validation Corporate Inn Sunnyvale
B106 Complaint Handling Complaint Handling, Medical Device Reporting, Removals and Recalls Corporate Inn Sunnyvale
B111 Risk Management Risk Management Corporate Inn Sunnyvale
B116 FDA, Notified Body and Internal Auditing Internal Auditing Corporate Inn Sunnyvale
B118 ISO 13485:2008 Implementation and Transitioning of the QMS for Medical Device Organizations ISO 13485:2008 Corporate Inn Sunnyvale
B119 International Regulatory Requirements (CE, CMMD,PAL, etc.) International Regulatory Requirements Corporate Inn Sunnyvale
B125 Document Control and Records Management in Regulated Environments Document Control Corporate Inn Sunnyvale
B133 Medical Device Design Verification & Validaiton Medical Device Design V & V Corporate Inn Sunnyvale
B112 Biomedical Design Control Requirements Design Control Requirements Corporate Inn Sunnyvale