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New EU regulations - MDR and IVDR

Get to know the new Medical Device and IVD Regulations - Prepare for the transition

On-line webinar
Completed 15 September 2017. Available as recording.

EU Medical Devices Regulation (MDR) and
In Vitro Diagnostic Medical Devices Regulation (IVDR)


On May 26 the new regulations entered into force and the transition periods begun.  Find out what this means for your company!


Course description:

The MDR and IVDR received a positive vote in the European Parliament on 5th April 2017. The final text has been published in the Official Journal and entered into force on May 26 this year. The transition period will span three years for medical devices and five years for IVD’s.

During this webinar we will briefly examine the background to the updated regulations and then provide an overview of the structure of the regulations and the most important differences in comparison to the current medical device directives. The impact of the regulation will be discussed, in addition to how to prepare for and manage the transition.

Who should attend:

Anyone in Senior Management, QA, QC, Regulatory Affairs, Product Development, Process development or Production that needs to understand the impact of the new regulations.

 

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Course facts

Course no:
5002
Industry:
Medical Devices

Level:
Intermediate
CS region:
EU

Language:
English
Instructor:
Åse Ek
Åse Ek

Date:
 
Completed 15 September 2017. Available as recording.


Time:
90 min

Price (excl. local VAT):

Recording: 190 Euro
Course handouts (PDF) included
No certificate.

For in-house live webinar, contakt us for an offer.


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