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Upskill/Reskill for work in MedTech
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Pharma/Biopharma
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Soft Skills
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
EU MDR
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
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)
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
Introduction to HACCP Classroom Training
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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Online training for 21 CFR 820 Subpart E – Medical Device Purchasing Controls
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