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