Training Features

Is Your Product a Medical Device?

This training is designed to provide actionable insights and practical guidance, helping your organization determine whether your product qualifies as a medical device under the EU MDR, ensuring proper classification and regulatory compliance.
Format

E-Learning

Level

Basic

Trainer

Mindy McCann

Exam

Exam and certificate included

Duration

2 hours and 50 mins.
12 modules

Price

€ 450 or equivalent currency

Comprehensive Regulatory Expertise

Enhance your expertise with our training program on determining if your product qualifies as a medical device in the EU. Develop the skills to excel as a regulatory professional and effectively navigate 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

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.
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