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Creating High-Quality Products: A Training Course for Manufacturing Professionals
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Failure Mode and Effect Analysis (FMEA)
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Audit preparation
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ISO 13485:2016 Clause by Clause
Introduction to 21 CFR 820 Quality System
CAPA in the Medical Device Industry
Project Management Skills for an Effective CAPA
Mastering EU MDR: Navigating Compliance for Medical Devices
How to Prepare for a FDA QSIT Inspection
How to Prepare for a Medical Device Single Audit Program (MDSAP)
ISO 14971:2019 Risk Management for Medical Devices Classroom Training
Annual cGMP Drug/Device Combination Products (21 CFR 820, ISO 13485:2016, CFR Part 4, 210 and 211)
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CGMP Essentials for the Pharma/Biopharma industry
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A3 Problem Solving Training Course
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FDA QSR & QSIT for Medical Devices: An Introductory Course
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Introduction to ISO 13485:2016 Training Course – 15th Jan 2024
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