-Prepare, review, and submit CTD/eCTD/ACTD dossiers for international product registrations.
-Ensure compliance with regulatory requirements in EU, US, Asia, CIS, LATAM, and Africa.
-Coordinate with regulatory agencies/client for product approvals.
📌 Drug Regulatory Affairs Executive New Delhi (India)
🏢 Vee Excel
📍 India
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.