Description : Conducting an effective root cause analysis can be a daunting task. And without a good root cause analysis, your CAPA will not result in the desired improvement. This webinar will give you insights and lessons learned from an industry expert with over 30 years’ experience. You will learn how to get permanent resolution to your serious quality problems. CAPA is the corner stone of an effective Quality System for Medical Device companies. However, it is still the number one cause of 483 and Warning Letter Observations. Without an accurate root cause analysis it is impossible to correct and prevent quality and compliance issues. Many companies struggle with inadequate root cause analysis resulting in on-going quality and compliance problems. This webinar will help you improve your root cause analysis leading to real and lasting improvements.

1. Contact Us
Email:david@grcts.com
Tel:+1-248-233-2049
Web:www.grcts.com
GRC Training Solutions

2.  Conducting an effective root cause analysis can be a daunting task. And
without a good root cause analysis, your CAPA will not result in the desired
improvement. This webinar will give you insights and lessons learned from
an industry expert with over 30 years’ experience. You will learn how to get
permanent resolution to your serious quality problems.
 CAPA is the corner stone of an effective Quality System for Medical Device
companies. However, it is still the number one cause of 483 and Warning
Letter Observations. Without an accurate root cause analysis it is impossible
to correct and prevent quality and compliance issues. Many companies
struggle with inadequate root cause analysis resulting in on-going quality
and compliance problems. This webinar will help you improve your root
cause analysis leading to real and lasting improvements.

3.  FDA Expectations
 A Methodical Process for Root Cause Analysis
 Root Cause Analysis Techniques
 Do's and Don'ts
 Myths of Root Cause Analysis
 Documentation Expectations

4.  Build the right team
Develop a problem statement
Data Collection
Analysis Tools and Techniques
How to Verify your Results

5.  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. 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.

6.  Live : For one participant
$179
 Corporate Offer 1 : Max 3 - 5 Participants
$499
 Corporate Offer 2: Max 10 Participants
$699
 Recorded Webinar: Get unlimited access to the link for six months
$ 229
 Get CD/DVD:
$339
 Super Combo Offer 1: For One partcipant Live and Recorded webinar Only!
$389
 Super Combo Offer 2: For One partcipant Live and Training CD Only!
$429.