When: Tuesday 26 February 2019, 14:00 - 15:00 AM CET
What: During this training, good practices to ensure the smooth and timely development of harmonised standards in support of the Medical Devices Directives and Regulations will be presented. Speakers will briefly present the new legislative framework related to Medical Devices (2017/745/EU and 2017/746/EU), clarify the content of the Annex(es) ZA/ZZ and the process for its/their provision during the standard development process (also for parallel work with ISO and IEC).
The webinar will also remind some practicalities regarding the involvement of HAS consultants in the standard development process.
Who: Technical Body Officers in the medical field, interested BT members and NSB/NC staff and identified sector representatives (liaisons, etc..)