Gestor certificado ISO 13485
The Certified Quality Manager Medical Devices is a 44-hour training program for 5 e-courses. ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management, U.S. FDA 21 CFR Part 820 QMSR Requirements 2026, Good Documentation Practice, and FMEA. 4.4 CEUs. Language: English.