Training Features

Determine the Regulatory Pathway

This training is designed to provide actionable insights and practical guidance, helping your organization identify and navigate the appropriate regulatory pathway under the EU MDR, ensuring compliance and efficient market access.
Format

E-Learning

Level

Basic

Trainer

Olena Hoi

Exam

Exam and certificate included

Duration

2 hours
7 modules

Price

€ 350 or equivalent currency

Comprehensive Regulatory Expertise

Enhance your regulatory expertise with our specialized training empowering you to determine the regulatory pathway for medical devices. Become a proficient regulatory professional, confidently navigating the evolving landscape of medical device compliance.
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.

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