Changes in the Medical Devices Regulation affect drug delivery devices

EAMONN HOXEY | July 10, 2017

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Article 117 of the Medical Devices Regulation (MDR) (Regulation (EU) 2017/745) amends the Directive on medicinal products for human use (MPD) (Directive 2001/83/EC). This will significantly affect pharmaceutical manufacturers supplying drug delivery devices in combination with their medicinal products (such as pre-filled syringes).

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