Struggling to understand the new EU MDR and IVDR? Join Theresa Jeary, Technical Services Manager Medical Devices Certification, LRQA Medical Directives Team, as she shares her view on the key changes. www.lrqausa.com | www.lrqa.com.br | www.lrqamexico.com

1. Improving performance,
reducing risk
New EU MDR and IVDR: Understanding Key
Changes, Impacts and Actions
Tuesday, Sept 20 at 2:45 – Exhibit Hall
Join this session for an understanding of the key changes,
impacts, transition phase and key steps to be taken around
this new EU MDR/IVDR Medical Device Law.
Don’t miss these sessions at:
Join Theresa Jeary,
Technical Services Manager
Medical Devices Certification,
LRQA Medical Directives Team,
as she shares her view on the
key changes.
Understanding ISO 13485:2016 – Risk
Management Implications and Interconnection
with Other Regulatory Requirements
Tuesday, Sept 20 at 3:30 – Room LL21 C/D
Find out what’s new and what has changed and the impact
it will have on your organization.
Tuesday, Sept 20 at 2:45 • Exhibit Hall
Struggling to
understand
the new EU MDR
and IVDR?
Visit LRQA at Stand #225
for a chance to win an
Amazon Echo®
or a
Fit Bit Blaze®
!