Key Take Away :
This webinar will discuss the essentials of Post Market Surveillance, how you can develop your capabilities and how PMS can provide you with important information to improve your device, better service your customers, and reduce the risk of adverse events.
Overview:
Post Market Surveillance (PMS) is the practice and system of monitoring the safety awareness training of a medical device after it has been released on the market.
It relies on several foundations including unique device identifiers (UDI), electronic health records and medical device reporting, device registries, and advance methods for evidence generation, data analysis and vigilance awareness training. It is a system that continues to develop and improve.
Why Should You Attend :
Post Market Surveillance is an essential part of the FDA’s mandate to protect the public health. This Post Market Surveillance and Vigilance Webinar will establish why it is something that every medical device company needs to understand to ensure product safety and effectiveness and customer satisfaction.
Areas Covered In This Webinar :
Overview and Definitions
FDA Expectations, Regulations
Lessons Learned and Enforcement Case Studies
Medical Device Reporting
Learning Objectives :
Investigating a complaint or MDR
FAERS – FDA Adverse Event Reporting System
Common Mistakes and how to avoid them
Best Practices
Preparing for an FDA or NB Inspection
Who Will Benefit :
Complaint Specialists and Managers
Individuals participating in Failure Investigations
Individuals analyzing Returned Products/Complaint Analysis
Regulatory Affairs Personnel
Quality Engineers
Clinical Affairs Personnel
Complaint Handling Unit Personnel
Compliance Specialists
For more information, please visit : https://www.atozcompliance.com/trainings-webinar/life-sciences/medical-devices/post-market-surveillance-and-vigilance-webinar-training/susanne-manz/300201
Email: support@atozcompliance.com
Toll Free: +1- 844-414-1400
Tel: +1-516-900-5509
Level:
Intermediate
Speakers Profile :
Susanne Manz
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.
Susanne has a BS in Biomedical Engineering and an MBA from the University of NM. She earned her Black Belt and Master Black Belt certifications while at Johnson and Johnson. Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality.
Susanne has now established a consulting business with a mission to provide services to help medical device companies achieve world-class quality and compliance.
This webinar will discuss the essentials of Post Market Surveillance, how you can develop your capabilities and how PMS can provide you with important information to improve your device, better service your customers, and reduce the risk of adverse events.
Overview:
Post Market Surveillance (PMS) is the practice and system of monitoring the safety awareness training of a medical device after it has been released on the market.
It relies on several foundations including unique device identifiers (UDI), electronic health records and medical device reporting, device registries, and advance methods for evidence generation, data analysis and vigilance awareness training. It is a system that continues to develop and improve.
Why Should You Attend :
Post Market Surveillance is an essential part of the FDA’s mandate to protect the public health. This Post Market Surveillance and Vigilance Webinar will establish why it is something that every medical device company needs to understand to ensure product safety and effectiveness and customer satisfaction.
Areas Covered In This Webinar :
Overview and Definitions
FDA Expectations, Regulations
Lessons Learned and Enforcement Case Studies
Medical Device Reporting
Learning Objectives :
Investigating a complaint or MDR
FAERS – FDA Adverse Event Reporting System
Common Mistakes and how to avoid them
Best Practices
Preparing for an FDA or NB Inspection
Who Will Benefit :
Complaint Specialists and Managers
Individuals participating in Failure Investigations
Individuals analyzing Returned Products/Complaint Analysis
Regulatory Affairs Personnel
Quality Engineers
Clinical Affairs Personnel
Complaint Handling Unit Personnel
Compliance Specialists
For more information, please visit : https://www.atozcompliance.com/trainings-webinar/life-sciences/medical-devices/post-market-surveillance-and-vigilance-webinar-training/susanne-manz/300201
Email: support@atozcompliance.com
Toll Free: +1- 844-414-1400
Tel: +1-516-900-5509
Level:
Intermediate
Speakers Profile :
Susanne Manz
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.
Susanne has a BS in Biomedical Engineering and an MBA from the University of NM. She earned her Black Belt and Master Black Belt certifications while at Johnson and Johnson. Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality.
Susanne has now established a consulting business with a mission to provide services to help medical device companies achieve world-class quality and compliance.
