Training Features
Clinical Investigations under the EU MDR
This training is designed to provide actionable insights and practical guidance, helping your organization understand and manage the requirements for clinical investigations under the EU MDR, ensuring compliance and robust clinical evidence for market approval.
Format
E-Learning
Level
Basic
Trainer
Bianca Lutters
Exam
Exam and certificate included
Duration
2 hours
15 modules
Price
€ 425 or equivalent currency
Comprehensive Regulatory Expertise
Gain expertise in Clinical Investigation with our in-depth training program, equipping you with the skills and knowledge to confidently conduct successful clinical trials.
Upon successful completion of the program, participants receive a recognized certification, boosting their career prospects and demonstrating their expertise to employers and clients.
Certification and Career Advancement
We offer a flexible learning schedule, allowing professionals to balance their training with their busy work and personal lives, ensuring accessibility to a wide range of learners.
Flexible Learning Schedule
Explore the training modules available in this course
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.
