Training Features

Understanding Governance Regulations under the EU MDR

Gain insight into governance requirements and regulatory responsibilities under the EU MDR with this focused training.
Format

E-Learning

Level

Basic

Trainer

Gert Bos

Exam

Exam and certificate included

Duration

45 minutes
4 modules

Price

€ 165 or equivalent currency

Comprehensive Regulatory Expertise

Discover our e-learning course and build your knowledge of EU medical device regulations anytime, anywhere, at your own pace.
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

Gert Bos

Gert Bos, a leading MDR expert with 26 years of experience across life sciences, academia, industry, and Notified Bodies, provides strategic regulatory and business consulting, supports due diligence processes, delivers in-house training on EU-MDR and EU-IVDR, and has held senior leadership roles at BSI and KEMA while actively contributing to RAPS, TEAM-NB, and EU regulatory workgroups.
Write your awesome label here.