Training features
Post-Market Clinical Follow-up (PMCF)
This training is designed to provide actionable insights and practical guidance, helping your organization implement and manage effective Post-Market Clinical Follow-up (PMCF) activities to comply with EU MDR requirements and support ongoing product safety and performance.
Format
E-Learning
Level
Basic
Trainer
Bianca Lutters
Exam
Exam and certificate included
Duration
2 hours
8 modules
Price
€ 345 or equivalent currency
Comprehensive Regulatory Expertise
Uncover the latest strategies and regulatory insights essential for maintaining medical device safety and performance. Join us to refine your PMCF process and stay ahead in ensuring compliance and effective post-market surveillance.
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.
