Courses
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Certified Quality Manager - Medical Devices [English]
3 CoursesThe 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, and FDA 21 CFR 820 cGMP Requirements. 4.4 CEUs. Language: English.
$995
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GMP Pharma Lead Auditor [English]
This ON DEMAND 40-hour e-course teaches an understanding of the requirements of FDA 21 CFR 210 and 211 Pharmaceutical CGMP, ISO 13485, and ISO 19011 Lead Auditing. Includes a certified training Certificate of Competence. 4.0 CEUs. Language: English.
$495
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GMP Pharma Internal Auditor [English]
This ON DEMAND 32-hour e-course teaches an understanding of the requirements of FDA 21 CFR 210 / 211 Pharma CGMP, ISO 13485, and ISO 19011 Internal Auditing. Includes a certified training Certificate of Competence. 3.2 CEUs. Language: English.
$395
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GMP Pharma 210-211 Requirements [English]
This ON DEMAND 8-hour e-course teaches a detailed understanding of the concepts and requirements of FDA 21 CFR 210 and 211 Pharmaceutical CGMP regulations. Includes a certified training Certificate of Competence. 0.8 CEUs. Language: English.
$395
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GMP Pharma - Training Bundle [English]
3 CoursesThe GMP Pharma training bundle includes three ON DEMAND e-courses, including GMP Pharma Lead Auditor ISO 14971 Risk Management Medical Devices Requirements, and Failure Mode and Effects Analysis (FMEA). Language: English.
$795
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Supplemental - Training Bundle [English]
4 CoursesThe Supplemental training bundle includes four ON DEMAND e-courses, including 5S - Steps to a Better Organization, Culture of Quality, Failure Mode and Effects Analysis (FMEA), and Good Documentation Practice (GDP). Language: English.
$495