Western Canada Chapter Virtual Event: From Remediation to Innovation: Leveraging EU-MDR Principles t

Although EU MDR is no longer “new”, many manufacturers are just starting to think about how to integrate MDR into their new product development (NPD) and sustaining activities. By embedding MDR principles product development processes, manufacturers have an opportunity to gain efficiencies across multiple regions, especially as it pertains to clinical evidence generation. This session aims to discuss the key considerations for process improvement and accelerating time to market in OUS regions by leveraging MDR requirements.

Registration Fees & Deadlines

Speakers

Dona O'Neil
Associate Director of Scientific Affairs at BD Interventional Surgery at Becton Dickinson

Substitutions

Paid registration substitutions may be accepted with written approval from RAPS for requests received before the start of the event. To transfer a registration, email support@raps.org with the event title, name of the original registrant and the contact information for the new attendee.

Proof of Attendance

A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.

Questions