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Webinar On Using Metrics to Monitor and Improve Your Quality Management System

 
  March 04, 2016  
     
 


Compliance Trainings, Online
2016-04-08


Description :

Medical Device companies need effective metrics and dashboards to ensure they are proactively and consistently meeting the needs of all their stakeholders:

Customers: It is critical to maintain metrics to ensure that your customers are receiving safe and effective products. Metrics that measure and trend product quality and customer satisfaction are critical. Fast or real-time systems are needed to ensure proper responsiveness.

Regulators: Proper metrics can help you identify, analyze, and mitigate compliance risks.

Business Stakeholders: Better decision making is enhanced by good data and information. Good metrics and scorecards help create a transparent environment where key indicators are proactively measured and addressed. Proper metrics should escalate and inform the appropriate levels of management, improving decisions on where to put resources.

Medical device companies face ever increasing scrutiny from the FDA and other regulators. Customers demand quality and safety. The business requires efficient and effective use of resources. Without proactive and timely metrics, a company is blind to the health of its quality system. This can lead to disaster for the company or, even worse, its customers.

Areas Covered in the Session :

How to create a balanced scorecard

How to move from lagging to leading indicators

How to use indices or profiles to create a more complete picture of performance

Lack of transparency in quality/compliance data

Use of metrics and dashboards for management review

Maturity levels in use of metrics

Scalability and hierarchy in metrics

Who Will Benefit:

Quality Assurance Managers

Quality Control Managers

Regulatory Affairs Teams

Compliance Managers

Individuals preparing data for Management Review

 

Directors, VPs, and others attending Management Review

 
 
Organized by: Compliance Trainings
Invited Speakers: Susanne Manz 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. She 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.

 
Deadline for Abstracts: 2016-04-08
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1635

 

To register this webinar

https://compliancetrainings.com/siteengine/Login.aspx 

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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