This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

MedTech Summit US

HURRY! $600 SAVINGS ENDS IN:

  • 00
    Days
  • 00
    Hrs
  • 00
    Mins
  • 00
    Secs
December 6 - 8, 2022
Intercontinental Chicago Magnificent MileChicago, IL

December 6 - 8, 2022
Intercontinental Chicago Magnificent Mile,
Chicago, IL

EU MDR Implementation

Notified Body Feedback. Industry Case Studies. Post Market Surveillance. Clinical Requirements

highlights include:

The very latest on EU MDR Implementation

  • Best practice EU MDR implementation industry case studies from Alcon and BTG International
  • Assess the common implementation challenges faced by manufacturers in our interactive panel discussion
  • Hear Notified Body and Competent Authority feedback on implementation so far

Gain answers to the questions keeping you awake at night

  • Will your Notified Body have sufficient capacity and resource? When and how can you switch your Notified Body?
  • ISO13485:2016 – Quality Management Systems QMS) and the MDR: what’s new and how can you prepare?
  • What are the expectations for clinical evaluations and investigations under the MDR?

Best practice industry perspectives and Notified Body insight from:

  • Medtronic
  • BD
  • Alcon
  • GMED North America
  • Zimmer Biomet
  • Abbott