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

NSF International, Pharmaceutical Services
Course summary
2 days
1,200 USD
English
Hamburg

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.

Expenses

Multiple participant and early bird booking discounts available. Discounts also offered to NHS staff, regulators and charities.

About provider

pharma training courses

NSF International provides a comprehensive range of independent, third-party pharmaceutical and biotech support services covering consulting, training, auditing and regulatory guidance for the pharmaceutical industry. These services are delivered by some of the most knowledgeable experts in their fields. Our unique...


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Contact info

NSF International, Pharmaceutical Services

The Georgian House, 22/24 West End
Kirkbymoorside
YO62 6AF York


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