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Quality Management Systems | FDA 21 CFR 820 QSR | Medical Device Quality - cGMP - Risk Management | Environmental Management Systems| All e-courses include a certified training Certificate of Competence
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The Medical Device - Certified Quality Manager CQM course bundle includes three ON DEMAND e-courses including ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management Requirements, and FDA 21 CFR 820 cGMP Requirements. 4.2 CEUs
The Medical Device - Certified Risk Manager CRM 8-hour e-course bundle includes two ON DEMAND e-courses including ISO 14971 Risk Management Medical Devices Requirements and FMEA Failure Mode and Effects Analysis. .8 CEU.
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 CEU.
(9) 4.9 average ratingThis 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. 6-hours / .6 CEU.
(4) 4.5 average ratingThis 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. 6-hours / .6 CEU.
(2) 4.5 average ratingThis ON DEMAND 32-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 9001 Quality Management standard and ISO 19011 Lead Auditing and includes certified training Certificate of Competence. 32-hours / 3.2 CEU.
This ON DEMAND 32-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 14001 Environmental standard and ISO 19011 Lead Auditing and includes a certified training Certificate of Competence. 32-hours / 3.2 CEU.
(1) 5.0 average ratingThis ON DEMAND 24-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 13485 Medical Quality standard and ISO 19011 Auditing and includes a certified training Certificate of Competence. 24-hours / 2.4 CEU.
This ON DEMAND 16-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 13485 Medical Device Quality Management standard and includes a certified training Certificate of Competence. 16-hours / 1.6 CEU.
(6) 5.0 average ratingThis ON DEMAND 15-minute e-course teaches a high-level preview of the ISO 13485 Medical Device Quality Management Systems standard. This course does not include a Certificate of Competence.
(4) 5.0 average ratingThis ON DEMAND 1-hour e-course teaches a very brief overview of key concepts and major requirements of the ISO 13485 Medical Device Quality Management standard and includes a certified training Certificate of Competence. 1-hours / .1 CEU.
This ON DEMAND 1-hour e-course teaches a very brief 1-hour overview of key concepts and major requirements of the ISO 14971 Medical Device Risk Management standard and includes a certified training Certificate of Competence. 1-hour / .1 CEU.
This ON DEMAND 15-minute e-course teaches a very brief overview of the ISO 14971:2019 Medical Device Risk Management standard and summarized key changes from the 2007 version. This course does not include a Certificate of Competence.
(1) 5.0 average ratingThis ON DEMAND 1-hour e-course is an annual GMP Overview of the Quality System Regulations (QSR) and cGMP required by the FDA for Medical Devices and includes a certified training Certificate of Competence. Continuous education 1-hour / .1 CEU.
(1) 5.0 average ratingThis ON DEMAND 15-minute e-course teaches a very brief overview of cGMP required by the FDA for Medical Devices. This course does not include a Certificate of Competence.
Overview | Requirements | Internal Auditor | Lead Auditor
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