Collection of Medical Device-related Mind Maps & Processes (click on the text to jump to the original articles)

01 Device-related Mind Map | Matters about Internal Audit and Management Review of Medical Devices (2023 Edition)

02 Device-related Mind Map | Matters about Sampling Inspections of Medical Devices (2023 Edition)

03 Device-related Mind Map | Matters about Human Resources in Medical Device Manufacturers (2023 Edition)

04 Device-related Mind Map | Mind Map for Rectification of Medical Device Production Quality Management System (Revision in August 2023)

05 Device-related Mind Map | Mind Map for Risk Sources and Standardized Management of Medical Device Registrants and Filing Parties (Revision in August 2023)

06 Device-related Mind Map | Mind Map for Medical Device Production Quality Control and Release (Revision in August 2023)

07 Device-related Mind Map | Mind Map for Overview of Medical Device Clinical Trials (2023 Edition)

08 Device-related Mind Map | Mind Map for Overview of Device-related Ethical Matters (2023 Edition)

09 Device-related Mind Map | Mind Map for Online Sales of Medical Devices

10 Device-related Mind Map | Management of Suppliers for Medical Device Manufacturers

11 Device-related Mind Map | Mind Map for Attributes and Regulation of Medical Device Products

12 Device-related Mind Map | Establishment and Operation of Medical Device Production Quality Management System

13 Device Operation Regulation | Mind Map for Regulation of Medical Device Operations (2023 Edition)

14 Device-related Process | Canadian MDL Registration Preparations and Certification Approval Process

15 Device-related Process | Mind Map for Warehouse Management of Medical Device Manufacturers (2023 Edition)

16 Device-related Process | Taiwan Medical Device Marketing Authorization Process

17 Device-related Process | Mind Map for Registration Inspection of Medical Device Production Quality Management System (2023 Edition)

18 Device-related Process | Mind Map for Reports of Medical Device Registrants and Filing Parties (2023 Edition)

19 Device-related Process | Medical Device UDI Basic Content and Implementation Process (Updated in March 2023)

20 Device-related Process | Mind Map for Management of Medical Device Adverse Event Monitoring, Reporting and Recall (2023 Edition)

21 Device-related Process | Mind Map for Punishment and Rectification of Medical Device Manufacturers

22 Device-related Process | Simple Mind Map for Medical Device Production Quality Management System (2023 Edition)

23 Device-related Process | Mind Map for GB9706.1 - 2020 Implementation and Supervision

24 Device-related Process | General Process of Medical Device Registration in Hong Kong

25 Device-related Process | Medical Device UDI Basic Content and Implementation Process (2023 Edition)

26 Device-related Process | Mind Map for Management of Medical Device Adverse Event Monitoring, Reporting and Recall (2023 Edition)

27 Update | Mind Map for Risk and Hazard Investigation by Medical Device Manufacturers (2023 Edition)

28 Device Application Process | Mind Map for Medical Device Clinical Trial Overview and Ethics Committee

29 Device Application Process | Workflow of Adverse Event Monitoring by Registrants and Filing Parties

30 Device Application Process | Changes in Filing and Changes in Registration of Domestic Class II Medical Devices

31 Device Application Process | Changes in Medical Device Production Licenses (Registration Matters + Licensed Matters)

32 Device Application Process | Issuance of Production Licenses for Domestic Class II and III Medical Devices

33 Device Application Process | Renewal of Production Licenses for Class II and III Medical Devices

34 Device Application Process | Issuance of Registration Certificates for Domestic Class II Medical Devices

35 Device Application Process | FDA 510K Registration Application

36 Device Application Process | EU CE Certification of Medical Devices

37 Device Application Process | Application for Medical Device Classified Demarcation

Source: Guangdong Food & Drug Technology Association for Evaluation & Certification