Training Features

The CE Certification Process under EU MDR

This training is designed to provide actionable insights and practical guidance, equipping your organization to navigate the CE certification process under the EU MDR, ensuring compliance and market access success.
Format

E-Learning

Level

Basic

Trainer

Olena Hoi

Exam

Exam and certificate included

Duration

1 hour and 40 mins.
6 modules

Price

€ 300 or equivalent currency

Comprehensive Regulatory Expertise

Enhance your expertise through our CE Certification training, equipping you to excel as a proficient regulatory professional adept at navigating the evolving terrain of medical device compliance aligned with CE certification standards.
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

Modules

Explore the training modules available in this course

Meet the Trainer

Olena Hoi

Olena is a seasoned Quality and Regulatory Affairs Consultant at Qserve Group with extensive experience in managing Quality Management Systems, conducting audits, and authoring regulatory submissions for high-risk medical devices across global markets, particularly in the EU under MDR and MDD regulations.