Certified Quality Manager | Medical Devices
The Certified Quality Manager Medical Devices is a 44-hour training program for three ON DEMAND e-courses. ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management Requirements, and FDA 21 CFR 820 cGMP Requirements. 4.4 CEUs.
V360 Training Advantages
ISO 13485:2016 Lead Auditor4.6
This ON DEMAND 32-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 13485 Medical Quality Management standard and ISO 19011 Lead Auditing and includes a certified training Certificate of Competence. 3.2 CEUs.
FDA 21 CFR 820 cGMP Requirements4.5
This ON DEMAND 6-hour e-course teaches the Quality System Regulations (QSR) and Current Good Manufacturing Practices (cGMP) required by the FDA for Medical Devices and includes a certified training Certificate of Competence. 0.6 CEUs.
ISO 14971:2019 Risk Management Medical Devices Requirements4.8
This ON DEMAND 6-hour e-course teaches a detailed understanding of the concepts and best practices of the ISO 14971:2019 Medical Device Risk Management standard and includes a certified training Certificate of Competence. 0.6 CEUs.
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