Webinar Features
Essential Tips & Tricks for Launching a Clinical Study under MDR
This on-demand webinar is designed to provide practical tips and actionable insights to help you effectively plan, execute, and manage clinical trials under EU regulations.
Format
On-Demand Webinar
Level
Basic
Trainer
Armêl Plaine
Exam
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
Access expert knowledge anytime with our on-demand webinar—flexible, convenient, and designed to fit your learning needs.
Watch on-demand webinars at your convenience, allowing you to fit learning into your schedule without missing essential information.
Flexible Viewing
Gain insights from industry experts and stay updated on the latest trends and regulations without the need to attend live sessions.
Access to Expertise
Meet the Trainer
Armêl Plaine
Armêl Plaine, PhD, brings over 14 years of expertise in clinical investigations for medical devices, specializing in high-risk devices across various clinical development stages, including First-in-Man, Exploratory, Confirmatory, and Observational Studies.
