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LIST OF TRAINING COURSES
Risk Management (ISO14971 : 2007)
Risk Management (ENISO14971:2012)
Process Validation
Post Market Surveillance, Vigilance and Adverse Event Investigation
Labelling of Medical Devices (ISO 15223-1)
Medical Device Classification
FMEA in medical device manufacturing
EU directives/ CE Marking
US FDA 21 CFR Part 820 (cGMP)
Effective Complaint Handling
Pre-Market Notification 510k Submissions Workshop
Australia Therapeutic Goods (Medical Devices) Regulations
ISO 13485 : 2016 Internal Auditing
ISO 13485 : 2016 QMS
Sterilization (EtO)
Sterilization (Gamma)
Malaysian Good Distribution Practice for Medical Devices (GDPMD)
Malaysian Good Distribution Practice for Medical Devices (GDPMD) Internal Auditing
US FDA Quality System Inspection Technique (QSIT)
CMDR and the Canadian Medical Devices Conformity Assessment System
Japan MHLW Ord 169
Developing Technical Documentation
Design of experiment
Excel Spreadsheet validation
Intellectual Property Rights in the medical device industry
Medical Device Design Control
Biological evaluations (ISO10993)
Clinical Investigations for Medical Technology
Lean Six Sigma Foundations
Lean Six Sigma Yellow Belt
Lean Six Sigma Green Belt
Lean Six Sigma Black Belt
Lean Foundations
Lean for Managers
Lean Enterprise
Lean for Manufacturing
Cross Functional Process Mapping
Process Control & Capability
Applied Statistics
Design for Six Sigma
Design for Lean Six Sigma
Level Pull & Kanban Design Workshop
Total Productive Maintenance
Achieving Results Through People
Lean Assessment
Value Stream Mapping
Problem Solving Skills
Business Process Improvement
Lean Six Sigma Champions Workshop
Lean Six Sigma Jumpstart Workshop
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Home
OUR SERVICES
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