Worked in internationally renowned pharmaceutical companies for more than 15 years, independently completing over 3000 electronic submission sequences of eCTD. Proficient in the technical requirements of eCTD in countries and regions such as the United States, the European Union, Switzerland, Canada, Australia, the Gulf region, Asia-Pacific region, South Africa, etc.
Proficient in using mainstream electronic document management systems (such as Veeva), electronic submission publishing tools and optimization tools of WORD and PDF.
Able to independently complete various types of electronic submissions other than eCTD, such as NeeS, ICH-CTD, ACTD, and the electronic submission publishing work for European medical devices.