Date: 30 January, 2025
Location: Virtual
Language: English
Introduction
Navigating the complexities of conducting clinical trials in the EU can be challenging, but with the right strategies, you can achieve compliance and streamline your process. This live webinar is designed to provide practical tips and actionable insights to help you effectively plan, execute, and manage clinical trials under EU regulations.
Join Armêl Plaine as she presents real-world advice and proven techniques to overcome common obstacles and ensure the success of your clinical trials.
The webinar consists of a 45-minute presentation and a live Q&A. Questions for the Q&A session can be sent in through the registration form, by email at marketing@qservegroup.com or during the webinar.
Learning Objectives
- Understand the key regulatory requirements for conducting clinical trials in the EU and how to ensure compliance with MDR.
- Learn best practices for efficient trial planning, patient recruitment, and data management tailored to the EU landscape.
Would Should Attend?
This webinar is ideal for professionals involved in clinical research and development, including:
- Clinical trial managers and coordinators
- Regulatory affairs and quality assurance specialists
- Sponsors and CRO representatives
- Startups and small-to-medium enterprises entering the EU market
Qserve Speaker