HI, I AM MICHAEL
I AM A NON-MAINSTREAM RA & A NON-PROFESSIONAL DEVELOPER
My everyday work is mainly on medical devices’ regulatory affairs, helping clients make regulatory strategies and/or prepare submissions for China NMPA and EU CE-Marking.
RA’s life sometimes is challenging, exciting, but we also feel helpless and boring. My goal is to make this kind of work easier and more efficient. To achieve the goal, I am trying to develop a management system and see if it helps.
This site will keep updating my new thoughts and experiments.
From start to finish, a beautiful website.
NMPA / CE-Marking / FDA
Strategy / Clinical / Lifecycle