7th Annual Medical Device Postmarket Surveillance Conference

February 23-25, 2021 | Virtual Event
Access Agenda

Pricing:
The entire course may be accessed for $1,500.

Target Audience:
Postmarket
Product Surveillance
Complaints
Risk Management

Industries Represented:
Medical Device
Diagnostic

Contact:

Rob Britt Photo

 

 

 

Rob Britt
Senior Event Manager
Q1 Productions
+1 (312) 224-8773
rbritt@q1productions.com

Improve Product Safety With Expert Interpretations Of Regulatory Updates To Effectively Analyze Data, Align Feedback With Quality Management Systems & Leverage Technology  

Ensure compliant data handling by benchmarking regulatory reporting requirements with peers. Dynamic presentations on operational readiness strategies to comply with EU MDR guidance, the impact of the MDSAP program on industry enforcement trends through the use of AI and automation tools for data mining will offer you takeaways for your own implementation. 

Join postmarket peers for direct insights and lessons learned from executive-level presenters. Attend collaborative group discussions and in-depth case studies live. Program content is made available on-demand after the event takes place so you can implement learnings within your own organization. 

The dynamic Q1 Productions virtual platform fosters a sense of collaboration. Thoughtfully designed networking features connect you with your peers beyond the capabilities of a Zoom meeting. Customize your experience and address your unique concerns during live Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session formats make it fun. Learning will take place in three half-day modules to maximize retention and engagement.

FAQ

Explore the Virtual Event Guide & FAQ for insight into our dynamic event platform, including technical requirements, audio troubleshooting, detailed networking steps and more. Our mobile app, Q1 Events, mirrors onsite networking experiences so you stay connected.

A Special Thanks to Our Sponsor:

""

The PMCF team at Purdie Pascoe have been providing Post Market Clinical Follow-up (PMCF) Survey solutions to medical device manufacturers since 2018. Purdie Pascoe can help with the PMCF plan / survey design, recruitment of end users, data collection and statistical reporting. The team are highly experienced in quantitative research, having conducted over 100 bespoke PMCF surveys for leading device manufacturers. The data we provide is used to support of the overall EU-MDR submission and has been reviewed and approved several Notified Bodies.  Our best-in-class approach is built upon previous market research experience, and is compliant with both GDPR and the Market Research Code of Conduct regarding anonymity.