Analyzing the Significance of eCTD Baseline Submissions
In the fast-evolving world of pharmaceuticals and Regulatory Affairs, the way companies submit their drug applications to health authorities is transforming. One of the key developments in this realm is the implementation of Electronic Common Technical Documents (eCTD) baseline submissions. These submissions have brought about a seismic shift in how Regulatory information is prepared, organized, and submitted to Regulatory agencies, and their significance cannot be overstated.