Post-Market Surveillance is a critical component to effective management of the Total Product Lifecycle of your device. The ultimate goal is to have conducted a thorough approach to design development and manufacturing such that the controls in place ensure the device will be safe and effective once on the market. Post-Market Surveillance is an avenue to provide further intelligence about your device and if it is meeting the expectations of your company. Even with the best design development and controls, there may arise an unintended impact to the patients and customers you serve. A proactive Post-Market Surveillance program will detect the issues and trends quickly and allow your company to react and improve the situation. In this first advanced webinar, the speaker will share best practices, data and strategies that will enable the you to enhance your current Post-Market Surveillance systems such that your system is proactive and is collecting meaningful intelligence to protect your company and your patients and customers.
This two-part series will focus on Advanced Post-Market Surveillance topics. We highly recommend (but not require) that you view the six-part Post Market Surveillance Series prior to this two-part advanced series in order to achieve maximum understanding and value. This series builds on and utilizes information shared in the Medical Device Reporting and Design Controls Series.
Each participant will receive a certificate of completion after each module attended upon the return of a completed evaluation form. Each participant will receive 0.1 CEU credits per hour of training.
Registrants may register for individual modules separately if desired. Select the module(s) of interest from the list provided above.
Who Should Attend:
All functions related to Quality and Regulatory Affairs, with specific focus on all systems that touch Post-Market Surveillance, such as Corrective Actions/Preventative Actions, Complaints, Investigations, and Recalls.