LIST OF TRAINING COURSES

1. Risk Management (ISO14971 : 2007)
2. Risk Management (ENISO14971:2012)
3. Process Validation
4. Post Market Surveillance, Vigilance and Adverse Event Investigation
5. Labelling of Medical Devices (ISO 15223-1)
6. Medical Device Classification
7. FMEA in medical device manufacturing
8. EU directives/ CE Marking
9. US FDA 21 CFR Part 820 (cGMP)
10. Effective Complaint Handling
11. Pre-Market Notification 510k Submissions Workshop
12. Australia Therapeutic Goods (Medical Devices) Regulations
13. ISO 13485 : 2016 Internal Auditing
14. ISO 13485 : 2016  QMS
15. Sterilization (EtO)
16. Sterilization (Gamma)
17. Malaysian Good Distribution Practice for Medical Devices (GDPMD)
18. Malaysian Good Distribution Practice for Medical Devices (GDPMD) Internal Auditing 
19. US FDA Quality System Inspection Technique (QSIT)
20. CMDR and the Canadian Medical Devices Conformity Assessment System
21. Japan MHLW Ord 169
22. Developing Technical Documentation
23. Design of experiment
24. Excel Spreadsheet validation
25. Intellectual Property Rights in the medical device industry
26. Medical Device Design Control
27. Biological evaluations (ISO10993)
28. Clinical Investigations for Medical Technology
29. Lean Six Sigma Foundations
30. Lean Six Sigma Yellow Belt
31. Lean Six Sigma Green Belt
32. Lean Six Sigma Black Belt
33. Lean Foundations
34. Lean for Managers
35. Lean Enterprise
36. Lean for Manufacturing
37. Cross Functional Process Mapping
38. Process Control & Capability
39. Applied Statistics
40. Design for Six Sigma
41. Design for Lean Six Sigma
42. Level Pull & Kanban Design Workshop
43. Total Productive Maintenance
44. Achieving Results Through People
45. Lean Assessment
46. Value Stream Mapping
47. Problem Solving Skills
48. Business Process Improvement
49. Lean Six Sigma Champions Workshop
50. Lean Six Sigma Jumpstart Workshop

CLICK HERE FOR TRAINING COURSE OVERVIEW

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