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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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CAPA
Audit preparation
Risk Management
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
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)
Pharma/Biopharma Industries Micro-Training Courses
CGMP Essentials for the Pharma/Biopharma industry
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ISO 9001:2015 Clause by Clause Classroom Training
Creating a Quality Culture
A3 Problem Solving Training Course
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ISO 22000 Clause by Clause Classroom Training
Effective Meeting Skills Classroom Training
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FDA QSR & QSIT for Medical Devices: An Introductory Course
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
Introduction to ISO 14971:2019 Risk Management for Medical Devices Training Course
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Introduction to ISO 9001:2015 Training Course – 21st September 2023
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