4th Annual Medical Device Postmarket Surveillance Conference

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January 17-18, 2018 – Arlington, VA

Event website: www.q1productions.com/postmarket-device/

This two day conference brings together executives who are responsible for product surveillance and reporting on a global scale to help ensure user feedback and complaints are handled appropriately and aligned with US and international regulatory requirements, streamlining and improving decision making, response times, and ultimately ensuring the safety and quality of medical products.

Don’t miss our presentation:

Thursday, January 18 – 4:45 pm

NOTIFIED BODY PERSPECTIVE OF UPDATED POSTMARKET REGULATIONS

  • New codes of conduct for notified bodies in European market
  • Impact of Brexit of UK registered notified bodies
  • NB collaborations with competent authorities
  • NB expectations of postmarket regulations in light of MDR

Presented by Salman Raza, Lead Assessor