Electronic submissions have taken the life science industry's Regulatory space by storm.
Submission excellence can bring benefits to organizations and enhance the ability to launch products more quickly.
China’s pharmaceutical industry has seen substantial growth since its entry into the World Trade Organization (WTO).
The process of submitting Regulatory documentation to Health Authorities can be complex and time-consuming.
eCTD submissions are one of the key steps in the development of pharmaceuticals.
Regulatory submissions and publishing tasks have traditionally been laborious involving hours of manual efforts for formatting documents,…
A multitude of challenges are faced by the Regulatory departments by the move from paper-based to eCTD submissions that continues around the world…
Since 2003, eCTD has been accepted by several Health Authorities around the world.
Pharmaceutical professionals in the Regulatory space face complicated, rigorous, and ever-evolving requirements for the Regulatory approval of…