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Introduction to 21 CFR 820 Quality System
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Project Management Skills for an Effective CAPA
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How to Prepare for a Medical Device Single Audit Program (MDSAP)
Annual cGMP Drug/Device Combination Products (21 CFR 820, ISO 13485:2016, CFR Part 4, 210 and 211)
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Mistake Proofing (Poka Yoke) Training
Failure Mode and Effect Analysis (FMEA)
Effective Technical Writing Skills
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Internal Auditor ISO 13485:2016 Training Course
Introduction to CAPA for Medical Devices Training Course
Introduction to ISO 13485:2016 Training Course
EU Medical Device Regulation (MDR) 2017/745 Fundamentals Training Course
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Introduction to ISO 13485:2016 Training Course – 7th June 2023
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