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Upskill/Reskill for work in MedTech
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Effective Technical Writing Skills
Creating High-Quality Products: A Training Course for Manufacturing Professionals
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Creative Problem Solving: Unlocking Innovation in Production Operations
Mistake Proofing (Poka Yoke) Training
Failure Mode and Effect Analysis (FMEA)
Medical Device Micro-Training Courses
Quality Systems
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
Quality Management Systems
Quality Culture
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ISO 9001:2015 Clause by Clause Classroom Training
Creating a Quality Culture
A3 Problem Solving Training Course
Introduction to HACCP Classroom Training
ISO 22000 Clause by Clause Classroom Training
Effective Meeting Skills Classroom Training
Medical Devices
Quality Management Systems
Food Safety Management (HACCP)
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
Internal Auditor ISO 9001:2015 Training Course
Introduction to ISO 9001:2015 Training Course
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Internal Auditor ISO 13485:2016 Training Course – 4th & 5th October 2023
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