Open Class Training Schedule
|
Date |
Training Course |
Period (day) |
|
2022.03 |
Regulation (EU) 2017/745 on medical devices |
2 |
|
2022.04 |
510(k) Premarket Notification |
2 |
|
2022.05 |
Medical Device Single Audit Program (MDSAP) |
2 |
|
2022.06 |
Regulation (EU) 2017/745 on medical devices |
2 |
|
2022.07 |
FDA CFR PART 820 Quality System Regulations Training |
2 |
|
2022.08 |
ISO13485:2016 Medical Devices--Quality Management SystemsRequirements |
2 |
|
2022.09 |
Regulation (EU) 2017/745 on medical devices |
2 |
|
2022.10 |
510(k) Premarket Notification |
2 |
|
2022.11 |
Medical Device Single Audit Program (MDSAP) |
2 |
|
2022.12 |
FDA CFR PART 820 Quality System Regulations Training |
2 |
