Irish Medtech Association’s Quality & Regulatory Forums represent important face to face information briefing sessions for QA/RA specialists in the medtech sector in Ireland.
Forum agendas are developed based upon Irish Medtech Association member feedback and in conjunction with the Chair and the Vice-chair of the Forum and members of Irish Medtech Association's Regulatory Steering Committee.
Over the last number of years, a major theme of Forum meetings has been the implementation of MDR and IVDR.
Forum participants have a unique opportunity to benchmark on wide ranging topical quality and regulatory issues and assess impact to business of same.
Typically, industry specialists from across Irish Medtech Association member companies and invited expert national and European speakers (including Notified Bodies/ Competent Authorities etc.) guide Forum participants through topics of interest.
QUALITY AND REGULATORY FORUM is an Irish Medtech Association MEMBER ONLY Event