4. Coordinate with other section for set action plan follow new regulation, advertisement process and OTH business flow.
Study FDA regultion, new medical device act of ThFDA
1. Update and gathering new medical device act and related regulation from ThFDA/ThMED and Asean with create tool/ procedure for develop RA system. 2. Attend the meeting of new FDA regulation Global guideline by ThFDA/ThMED/Other BC (5 times/PB) with make the meeting report and share to manager and RA member. 3. Coordinate with OSP and other BC for change notification response, keep record and share to RA member 4. Coordinate with other section for set action plan follow new regulation, advertisement process and OTH business flow.