Course description
European Medical Device Regulation (EU MDR)- Understanding and Implementing the Requirements
This two-day course provides comprehensive instruction on the European Union Medical Device Regulation (EU MDR) 2017/745. The course walks students through every aspect of the regulation and identifies key topics and changes, including the new roles associated with EU MDR, standard requirements that must be met by all manufacturers regardless of class and the requirements for conformity assessments. The course also provides premarket and postmarket requirements of conformity assessment.
Upcoming start dates
Training Course Content
Upon completion, students will be able to:
- Recognize the regulatory background in Europe,
- Identify the roles associated with the EU MDR,
- Discuss the Manufacturing Requirements of the EU MDR and
- Explain how to comply with premarket and postmarket requirements for conformity assessments.
Why choose NSF International, Health Sciences
Trained over 1,300 delegates on our CQI and IRCA certified GMP PQS lead auditor training course
Provided expert health sciences training for over 30 years
More people have become ‘Qualified Persons’ in Europe through our training programme than any other training provider
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Expenses
Multiple participant and early bird booking discounts available. Discounts also offered to NHS staff, regulators and charities.