Post-Market Surveillance Module 6: Operationalizing Post-Market Surveillance in a Global Company

Managing a global post-market surveillance system is extremely challenging in order to meet the constantly evolving global regulatory expectations. This final course combines lessons learned throughout the series to discuss how they work together to make a functional post-market surveillance system. Case studies are used to demonstrate industry challenges as well as best practices. A panel of experts take part in a question and answer session.

 

Expert Faculty

Patrick Caines
Director, Product Surveillance
GE Healthcare

Sharon Kapsch
Chief, MDR Policy Branch, Office of Surveillance and Biometrics
Center for Devices and Radiological Health, FDA

Steve Niedelman
Lead Quality System & Compliance Consultant
King & Spalding

Catherine Ricketts
Nurse Analyst
FDA

Richard Roy
Postmarket Surveillance Director
GE Healthcare

(Expert faculty titles and companies may have changed since the time of recording.)
 

Level

Intermediate
 

Learning Impact

Upon completion of this training, participants will:

  • Gain knowledge to implement a successful global post-market surveillance strategy
  • Possess tools to implement best practices


Certification

Certificate of Completion: Each participant will receive a Certificate of Completion for .1 CEUs upon viewing the webinar course and returning a completed evaluation form.
 

Price

$99 per module
$500 for entire series (Receive a 15% discount for purchasing all six modules)