1. GRM Roadmap
2. Guideline of GrevP
3. Guideline of GSubP
4. RAPS on-line courses

- Effective regulatory communication
http://raps.org/EventDetail.aspx?id=20846
- Role of the regulatory profession
http://raps.org/EventDetail.aspx?id=19094
- Project management for regulatory professionals
http://raps.org/EventDetail.aspx?id=19109

5. More references

- The 2011 APEC Good Review Practice on medical Products. The Basic GRevP Workshop (Oct. 12th-14th)
- The 2012 APEC Advanced Workshop of Good Review Practice on Medical Products (Nov.6th-8th)
http://www.fda.gov.tw/EN/site.aspx?sid=3309
- The 2015 International Good Submission Practice workshop on Pharmaceuticals
http://edu.tcfst.org.tw/edm/gsp/GSP.html