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European Medical Device Regulation (EU MDR)- Understanding and Implementing the Requirements

Length
2 hours
Price
399 USD excl. VAT
Next course start
Start anytime See details
Course delivery
Self-Paced Online
Length
2 hours
Price
399 USD excl. VAT
Next course start
Start anytime See details
Course delivery
Self-Paced Online
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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

1 start date available

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  • Self-Paced Online
  • Online
  • English

Training Course Content

Upon completion, students will be able to:

  1. Recognize the regulatory background in Europe,
  2. Identify the roles associated with the EU MDR,
  3. Discuss the Manufacturing Requirements of the EU MDR and
  4. 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.

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