Training

MedXview products included both desktop solutions and Web server based solution -- an enterprise content management and submission publishing tool that today’s complex regulatory environment demands. MedXview consistently delivers superior overall quality and functionality. We help your company in several key area such as:

Compliant with the latest international regulatory guidelines
Meets the stringent standards required by regulations like 21 CFR Part 11, the common technical document (CTD for paper submission) and the electronic common technical document (eCTD), Sarbanes-Oxley.

All-inclusive
All submission types supported such as eCTD, eIND, eNDA, eBLA, MAA, Paper CTD etc.
ALL regions supported for worldwide application include US, EU, Japan, and Canada

We help China, India, South America countries to get FDA and EMEA approval