EU MDR 2017/745
PQMS Academy Course
EU MDR 2017/745
European Medical Device Regulation Training
Training on EU MDR 2017/745 requirements for medical device quality and regulatory compliance.
2 Days
Medical Device Regulation Training
Designed for learners completing Medical Device Regulation for EU MDR 2017/745.
Who This Training Is For
- Quality, regulatory, operations, and improvement professionals
- Internal auditors, audit team members, and process owners
- Managers responsible for compliance, performance, and continual improvement
What Learners Will Cover
Program Requirements
Core concepts, terminology, expectations, and practical application for EU MDR 2017/745.
Practical Application
How learners can apply the training to real quality, regulatory, audit, or improvement activities.
Process Improvement
Ways to strengthen systems, evidence, controls, and follow-up actions after training.
Learner Readiness
Preparation for applying the course material in day-to-day work and team settings.
Course Outcomes
- Understand the purpose and structure of EU MDR 2017/745
- Apply course concepts to practical workplace scenarios
- Support compliance, audit readiness, and process improvement
Interested in EU MDR 2017/745 Training?
Contact PQMS Academy for course availability, scheduling, learner registration, and custom group training options.
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