In 2016, the European Commission published new harmonized standards for devices, implants and IVDs. Medical device manufacturers who market products in the EU must comply with these standards to enter the market.
Engage with regulatory colleagues from the Boston area for dinner and an interactive presentation on how to navigate harmonized standards in the EU.
The program is brought to you by the RAPS Boston Chapter and is intended to promote knowledge sharing and engagement with other in the local regulatory community.
RAC holders may claim two RAC recertification credits.
Regulatory Affairs Professionals Society (RAPS)5635 Fishers Lane, Suite 400Rockville, Maryland 20852
raps@raps.org+1 301 770 2920
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