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New EU regulations - MDR and IVDR

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

Recorded webinar

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

On May 26, 2017 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 April 5th 2017. The final text has been published in the Official Journal and entered into force on May 26th 2017. 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:
Medical Devices

CS region:

Åse Ek

Recorded 15 September 2017.

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File format:
Fil size:
80 MB

90 min

Price (excl. local VAT):

Recording: 250 Euro
Course handouts (PDF) included
No certificate.

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