---
title: "The Emergency Room Reality of Neurology Device Trials: A Planning Guide for Sponsors, Through the Eyes of the Sites Running Their Studies"
description: "A practical, site-led guide to planning neurology device trials around the realities of emergency-room screening, consent, workflow integration and after-hours coverage."
url: https://qbdgroup.com/en/webinars/emergency-room-reality-neurology-device-trials
type: "Webinar"
language: en
published: 2026-09-30
author: "Sophie Achten"
category: "Clinical Solutions"
publisher: "QbD Group"
citation: "QbD Group, \"The Emergency Room Reality of Neurology Device Trials: A Planning Guide for Sponsors, Through the Eyes of the Sites Running Their Studies\", https://qbdgroup.com/en/webinars/emergency-room-reality-neurology-device-trials"
---
# The Emergency Room Reality of Neurology Device Trials: A Planning Guide for Sponsors, Through the Eyes of the Sites Running Their Studies
> A practical, site-led guide to planning neurology device trials around the realities of emergency-room screening, consent, workflow integration and after-hours coverage.

_How emergency-care realities shape neurology device trials, from screening to follow-up_

🕐 3 PM CET

## About This Webinar

Neurology device trials often depend on decisions made in one of the most demanding clinical environments: the emergency room. Time pressure, rapidly changing patient conditions and complex hospital workflows can all affect screening, enrolment and study execution.

In this 60-minute webinar, QbD Group brings the site perspective into the planning process. Drawing on first-hand clinical operations experience, Sophie Achten explains the practical challenges sponsors should anticipate when designing and running neurology device studies in emergency-care settings.

The session focuses on four recurring operational challenges: time pressure during enrolment, informed consent in emergencies, integration into emergency-room workflows and continuity during after-hours coverage. It translates these realities into concrete planning considerations sponsors can use before their study reaches the site.

## What You'll Learn

- How emergency-room workflows influence screening and enrolment in neurology device trials
- Why informed-consent planning requires special attention in time-critical situations
- How to integrate study procedures into existing clinical workflows without overburdening site teams
- What sponsors should consider when planning after-hours coverage and rapid-response pathways
- How earlier site involvement can reduce avoidable delays and operational friction

## Speakers

### Sophie Achten

**Senior Clinical Project Manager · QbD Group**

Sophie Achten brings hands-on clinical operations experience to the planning and delivery of medical device studies. She helps sponsors translate study requirements into practical site workflows, with particular attention to feasibility, coordination and execution in complex care environments.

## Who Should Attend

- Clinical Operations Directors and Clinical Trial Managers at neurology MedTech companies
- Regulatory and clinical leaders planning neurology device studies in Europe
- MedTech founders and scale-ups preparing first-in-human or pivotal studies
- Hospital investigators and research teams involved in emergency-care studies
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Source: https://qbdgroup.com/en/webinars/emergency-room-reality-neurology-device-trials — © QbD Group. Quote freely with attribution and a link back.