Preparing for the eCTD Mandate

Join our FREE educational webinar to see what the implications of PDUFA V are, in particular the mandate to convert all regulatory submissions to eCTD.

Learning Objectives:
-Understand PDUFA V's repercussions on regulatory submissions

-Learn the steps needed to move from paper to electronic submissions (eCTD)
-Realize the advantages of direct communication with the FDA during the approval process