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  • 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