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
Bianca Lutters
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
Bianca Lutters
Bianca is a seasoned professional with over 15 years in the medical devices field, specializing in regulatory strategy, quality management, and clinical evaluation across diverse device categories, including high-risk cardiovascular products, and holds advanced degrees in medical biology and biochemistry.
