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Case Studies of MDD and MDR Audit Findings and Lessons Learned, an R&Q webinar

June 2 @ 1:00 pm - 2:00 pm

R&Q‘s March 2020 webinar focused on EU MDR audit findings. Feedback from that webinar indicated you wanted to see more case studies. We heard you loud and clear.

This webinar scheduled for Tuesday, June 2nd, will be completely focused on specific case studies of audit findings and lessons learned from both recent MDD and MDR audits.

R&Q is supporting many medical device companies with their transition from MDD to MDR. These companies span a wide range of clinical specialties, notified bodies, and geographic locations. R&Q’s involvement in client notified body audits and remediation efforts, as well as conducting internal and mock MDD/MDR audits for device companies, provides us with a significant amount of audit data and notified body perspectives.

In this webinar, we’ll present case studies of audit findings by functional area (risk management, post-market surveillance, etc.), along with where to expect notified bodies to focus.

The objective of this webinar is to arm you with audit prep information, so you can focus your resources on the right things and achieve MDR certification.

And for even more notified body perspectives, this webinar will be presented by R&Q’s Dr. Ibim Tariah, former BSI Technical Director of Medical Devices through 2019.

Click here to register

Details

Date:
June 2
Time:
1:00 pm - 2:00 pm
Event Categories:
,
Website:
https://www.rqteam.com/blog/case-studies-mdd-mdr-audit-findings

Venue

Online Event
OH United States

Organizer

Regulatory and Quality Solutions
Phone:
(877) 652-0830
Website:
http://www.rqteam.com/

BioOhio

Additional Event Details
BioOhio Member Event