Datasheet | October 30, 2023

Regulatory Operations Support


Halloran excels in Regulatory affairs, encompassing eCTD submissions. Our adept team is fully equipped to address your document preparation requirements, covering document formatting, PDF publication, eCTD compilation, and submission through the FDA's Electronic Submissions Gateway (ESG). Annually, Halloran handles thousands of submissions, spanning from new drug applications to ongoing lifecycle submissions.

If you already have an eCTD publishing vendor but require document formatting assistance, our dedicated team at Halloran offers document preparation support for numerous clients, extending to nonclinical reports and clinical study reports.

access the Datasheet!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.


Subscribe to Clinical Leader