Design and Development Requirements for Medical devices Training – CEMB
On March 29-30, 2021, Parivat Akarapimarn, Senior Consultant, participated as a speaker in the training of “Design and Development Requirements for Medical Devices” in collaboration with Center of Excellence on Medical Biotechnology (CEMB). The aim of this 2 day special training program is intended as an introductory course to provide participants to have a basic understanding of
- design and development requirements (design control) and its benefits,
- design control from a regulatory perspective,
- phases of design control,
- elements of design control and their execution,
- to develop skills for preparation of design history file
