ISO 13485 Lead Auditor / U.S. FDA CFR Part 820 QMSR
This bundle includes two courses: ISO 13485 Lead Auditor and U.S. FDA 21 CFR Part 820 QMSR 2026 Requirements.
Courses Included
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ISO 13485:2016 Lead Auditor [English] Exemplar Global Certified-26
This ON DEMAND 32-hour e-course teaches an understanding of the 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. Language: English.
$1,595
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U.S. FDA 21 CFR Part 820 QMSR 2026 Requirements [English]-26
5.0This ON DEMAND 2-hour e-course teaches a detailed understanding of the requirements of U.S. FDA 21 CFR Part 820 QMSR 2026 and CGMP regulations for Medical Devices. Includes a Certified Training Certificate of Competence. 0.2 CEUs. Language: English.
$695