6th Annual Medical Device Post-Market Surveillance Conference

January 22-23, 2020 | Alexandria, VA

6th Annual Medical Device Post-Market Surveillance Conference
January 22-23, 2020 | Alexandria, VA

Download Overview

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“I really appreciated the meeting. In my opinion it was even better than last year. Very high quality and good discussions.”

Manager Post-Market Studies EMEA
Abbott Medical Optics

“The quality of the speakers and presentations exceeded my expectations. I enjoyed the conference very much.”

Vice President, Regulatory Affairs & Quality Assurance
Aesculap

“I really believe this conference was top-notch. I must say you do a fantastic job in coordinating and producing these events, and I’ve been a part of many. I thought the conference exceeded expectations.”

SVP, Regulatory Affairs & Quality Systems
Renal Solutions

“You arranged a great cross-section of topics.”

VP Product Labeling & User Documentation
Siemens Healthineers

“Love the breakouts, workshops and discussion opportunities with peers.”

Director, Human Factors
Intuitive Surgical

About the Conference:

The medical device and diagnostic industries manufacture products that are amongst the most heavily regulated in the world’s marketplace due to the implications the performance of these products have on patient safety. Regulators around the world are looking beyond the safety and quality information submitted during initial product approval dossiers, but looking at the long term efficacy of devices through analyses of postmarket data compiled throughout a product’s entire lifecycle. Through case study driven presentations and collaborative group sharing, postmarket surveillance executives will be better equipped to understand best practices in PMS data collection, risk remediation strategies and remaining current on regulatory enforcement trends.​

Core Topics to be Addressed:

  • Further implementation strategies for EU MDR readiness
  • Postmarket surveillance processes for legacy devices
  • Securing product efficacy through stringent cybersecurity
  • Postmarket surveillance data reliability and usability
  • PMS considerations for a globally market product
  • Evaluation of current postmarket complaint escalation

Program Highlights:

  • Variety of perspectives including manufacturers and legal
  • Collaborative environment that fosters interactive engagement
  • Program focus will include both US/FDA and e-US discussions

Core Topics to be Addressed:

  • Further implementation strategies for EU MDR readiness
  • Postmarket surveillance processes for legacy devices
  • Securing product efficacy through stringent cybersecurity
  • Postmarket surveillance data reliability and usability
  • PMS considerations for a globally market product
  • Evaluation of current postmarket complaint escalation

Download Overview

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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