Eileen Ryan

submission services ectd Acorn Regulatory

The 3 Options for eCTD Publishing & Submission Services

The transition from paper-based submissions to the more costly eCTD system has caused many companies to reconsider how they undertake… Read more

UUID Numbers How To Fix

How To Fix Complications with UUID Numbers in eCTD

Acorn Regulatory’s publishing team is staffed by eCTD experts.  We have assisted many companies in their eCTD projects in recent… Read more

Esseential Guide To eCTD Electronic Publishing

Acorn Regulatory’s Essential Guide to eCTD & Electronic Publishing

We have worked with companies around the world on electronic publishing and eCTD issues for many years.  Acorn Regulatory has… 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

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

How To In-Licence An eCTD Dossier

We are taking a look at 4 factors to consider when planning to in-licence an eCTD dossier. When acquiring an… Read more

Your eCTD Questions Answered

Acorn Regulatory’s publishing team is staffed by eCTD experts.  We have assisted many companies in their eCTD projects in recent… 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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