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
Courses Included
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ISO 13485:2016 Lead Auditor
4.6This 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.
$495
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FDA 21 CFR 820 cGMP Requirements
4.5This 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.
$395
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ISO 14971:2019 Risk Management Medical Devices Requirements
4.8This 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.
$295
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Digitally verifiable certificates issued by a trusted global training provider.
Course Categories
Lead Auditor | Internal Auditor | Requirements | Overview
Globally recognized and trusted online training provider for leading medical device customers
International Accreditation
Our courses are designed to International Standards for Educational and Training Organizations.
