Open Class Training Schedule
Date | Training Course | Period (day) |
2020.03 | Regulation (EU) 2017/745 on medical devices | 2 |
2020.04 | 510(k) Premarket Notification | 2 |
2020.05 | Medical Device Single Audit Program (MDSAP) | 2 |
2020.06 | Regulation (EU) 2017/745 on medical devices | 2 |
2020.07 | FDA CFR PART 820 Quality System Regulations Training | 2 |
2020.08 | ISO13485:2016 Medical Devices--Quality Management SystemsRequirements | 2 |
2020.09 | Regulation (EU) 2017/745 on medical devices | 2 |
2020.10 | 510(k) Premarket Notification | 2 |
2020.11 | Medical Device Single Audit Program (MDSAP) | 2 |
2020.12 | FDA CFR PART 820 Quality System Regulations Training | 2 |