Wednesday, February 27th
12pm-1pm EST
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