Expert Profile
Dev Raheja
Risk Management Consultant, Independent
Dev Raheja, MS,CSP, author of the books Preventing Medical Device Recalls, Design for Reliability, and Assurance Technologies, is an international risk management, reliability, and system safety consultant for government, commercial and aerospace industry for over 30 years. His clients include Army, Navy, Air Force, NASA, Siemens, Eaton, Boeing, Lockheed, Northrup Grumman, General Motors, Prior to becoming a consultant in 1982 he worked at GE as Supervisor of Quality Assurance/Manager of Manufacturing Engineering, at Cooper Industries as Chief Engineer, and at Booz-Allen & Hamilton as Risk Management consultant for variety of industries. He teaches Design for Reliability courses at the University of Maryland for degree programs in Mechanical Engineering and Reliability Engineering. He is a Fellow of American Society for Quality and recipient of its Austin Bonis Award for Reliability Education Advancement, and former chair of the Reliability Division. He is a Senior Member of IEEE. He is a former National Malcolm Baldrige Quality Award Examiner in the first batch of examiners. His served as Vice president of the International System Safety Society where he received the Scientific Achievement Award and the Educator-of-the-Year Award. He served on the Board of Directors for the Annual Reliability and Maintainability Symposium for more than 10 years.
Trainings by Expert
3hr Virtual Seminar on Designing Medical Device Software to Prevent Product Recalls
Category:
Medical Devices
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Crisis Management
,
Life Sciences
,
Documentation and Data Management
4-hr Virtual Seminar: Design Reviews for Efficiency and Efficacy
Category:
Medical Devices
,
R & D
,
Research & Development
,
Device R & D
,
Life Sciences
Full Day Virtual Seminar: Reliability Engineering Fundamentals for Medical Devices
Category:
Medical Devices
,
R & D
,
Research & Development
,
Device R & D
,
Life Sciences
Designing Medical Device Alarms to Mitigate New FDA Concerns
Category:
Medical Devices
,
Audit
,
R & D
,
Research & Development
,
Device R & D
,
Life Sciences
Verification and Validation (V&V) of Software in the Medical Devices
Category:
Medical Devices
,
Life Sciences
,
Documentation and Data Management
Medical Device: Risk Assessment and Mitigation through FMEA
Category:
Medical Devices
,
Crisis Management
,
Life Sciences
The Use and Mis-use of FMEA in Medical Device Risk Management
Category:
Medical Devices
,
QMS, ISO 13485, CAPA
,
Life Sciences
Top 10 Medical Device Regulations Training (10 Courses)
Category:
Medical Devices
FDA Guidance on RUO (Research Use Only)/IUO (Investigational Use Only) Products
Category:
Medical Devices
,
Clinical Research
,
Laboratory Compliance
,
Risk Management
,
IVD
,
QMS, ISO 13485, CAPA
,
R & D
,
Laboratory
,
Clinical Trial Regulations
,
Research & Development
,
Device R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Designing Medical Devices for Safety with High Return on Investment
Category:
Medical Devices
