Eileen Ryan

eCTD Electronic Publishing Acorn Regulatory

Outsourced eCTD Publishing Services: An Overview

More countries are implementing eCTD.  As a result, more companies are being forced to make decisions regarding how they manage… Read more

PSUSA Deadline How To Guide

How To Prepare For A PSUSA Deadline

Do you have a PSUR Single Assessment (PSUSA) submission deadline approaching?  If so, our Regulatory Publishing Manager, Eileen Ryan, has… Read more

What To Consider When Planning To In-Licence An eCTD Dossier?

In this article we are taking a look at 4 factors to consider when planning to in-licence an eCTD dossier…. Read more

Your eCTD Questions Answered

Acorn Regulatory’s publishing team are eCTD experts.  We have assisted many companies in their eCTD projects in recent years.  Many… Read more

DMF Deadline

The US FDA DMF Deadline: 5 Things You Need To Know

The transition from paper based submissions to electronic Common Technical Document (eCTD) has continued in recent years.  This is something… Read more

Contact us and enjoy a faster, smoother journey through the maze of European Pharmaceutical and Medical Device legislation with us as your expert guide.
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