Join us for a webinar on July 10 for a discussion of the webinar 

Webinar Includes : All the training handouts , certificate ,Q/A and 90 mins Live Webinar

This webinar will explore tools for improving your Quality Management System. CAPA (Corrective and Preventive Action), Root Cause Analysis, Risk Assessment, Six Sigma, Management Review and more are processes that should be in your Quality Management System. Many companies have weak processes or understand these processes individually but they don’t know how to put them together into an efficient and effective program for continuous improvement. So, they continue to try new things in the hope that they will find something that sticks. 

In this webinar, we will discuss how to create a comprehensive system for continuous 

improvement including: 

  • Techniques to identify and prioritize risks 
  • Improvement methods with pros and cons 
  • Root Cause Analysis overview 
  • Project and change Management 
  • Control and monitoring 

Webinar Takeaways

 This 90-minute webinar will include: 

  •  Using a structured program to identify problems and opportunities for improvement 
  • How a culture of quality and compliance can encourage clear and transparent 
  • communication of risk. 
  • How to prioritize, resource, and implement corrective actions. 
  • Root Cause Analysis overview. 
  • Tools for monitoring and communicating risk and improvement over time.   
  • How to identify residual risk. 
  • Monitoring and Controlling progress over time. 
  • Signs that your company culture is taking unnecessary compliance or quality risk. 
  • How to ensure management gets valuable information to enable adequate 
  • prioritization and resourcing 
  • How to prioritize, resource, and implement corrective actions. 
  • Tools for monitoring and communicating risk and improvement over time.   

Can't Make this LIVE Webinar?

Simply select the Recorded option when registering and we will send you the link to view the recorded version.

Who Will Benefit

  • Quality Systems Specialists 
  • Document Control Specialists 
  • Quality and Compliance Specialists 
  • Auditors 
  • Auditor Managers 
  • Supplier Auditors 
  • Training Specialists 
  • CAPA Specialists 
  • Quality/Compliance leaders, managers, or directors for Medical Device companies 
  • General Managers wanting to learn about effective Management Review  

Industries who can attend

This 90-minute online course is intended for professionals in the Medical Device, Biotechnology,Pharmaceutical Industry. Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.

Faculty 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. While at GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, WW Director of Quality Engineering and, Design Quality, and Director of Corporate Compliance.

Faculty Susanne Manz

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