Training Features
What is the Classification of Your Medical Device?
Learn how to accurately classify your medical device with our expert-led online training, ensuring regulatory compliance and market success.
Format
E-Learning
Level
Basic
Trainer
Mindy McCann
Exam
Exam and certificate included
Duration
2 hours and 25 mins.
7 modules
Price
€ 395 or equivalent currency
Comprehensive Regulatory Expertise
Master the intricacies of medical device classification in our comprehensive online training, guiding you through EU MDR requirements with ease.
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
Mindy McCann
Mindy brings over 15 years of international Regulatory Affairs experience to Qserve, specializing in European, Canadian, and Australian medical device regulations and quality management systems.
Write your awesome label here.
