Effective Corrective and Preventive Actions (CAPA): 10 Steps

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    Live Webinar          on
 
     Effective Corrective and Preventive Actions (CAPA): 10 Steps

                                                                                                                                     
     Course "Efficient Effective Corrective and Preventive Actions
     (CAPA): 10 Steps" has been pre-approved by RAPS as eligible
                                                                                                 Register Now                        
     for up to 1.5 credits towards a participant's RAC recertification
     upon full completion.


    Date & Time:                                                                            Instructor Profile:

     Thursday, June 7, 2012              10:00 AM PDT | 01:00 PM EDT
                                                                                                         Jasmin NUHIC
     Duration: 90 Minutes                Instructor: Jasmin NUHIC                                    Sr. Compliance Quality
                                                                                                      Engineer, Medtronic
     Location: Online                    Price : $245.00   (for one participant)

                                                                                            Jasmin NUHIC serves a major
                                                                                            medical devices OEM as a Sr.
    Overview:                                                                               Compliance Quality Engineer and 21
    This CAPA training program helps you to understand, in 10 easy                          CFR Part 11 Subject Matter Expert.
    steps, the entire CAPA process. It includes elements of Quality Tools,                  He also served ASQ section as a
    Team Effectiveness, Awards & Recognitions, and Verification &                           chair for two consecutive terms, has
                                                                                            taught quality certification exam
    Validation of actions taken. Attend this webinar to grasp the A to Z of
                                                                                            prep course, completed numerous
    CAPA and learn how to implement & manage it for success.
                                                                                            software validations and obtained
                                                                                            over 25 different certifications in
    Why Should You Attend:                                                                  leadership, quality, software
                                                                                            validations, and more. Jasmin NUHIC
    We have found out, through auditing many organizations world-wide                       has conducted Webinars on this and
    that the organizations are pretty good when it comes to corrective                      other topics with high attendance
    actions yet they are not nearly as good when it comes to the                            and appreciation. ...more
    preventive actions. This webinar should provide you with enough
    ideas, suggestions and HOW TOs that you and your teams and
    organization overall get much better on the preventive actions and                     Suggest a Topic       More Webinars
    even better on the corrective actions. Includes all elements of CAPA
    process step as required by ISO and regulatory agencies.                                 Your Necessity is our Priority


    In addition, it is represented in a practical and proven manner which
    can be immediately applied in your organization.


    Areas Covered in the Session:                                                                             


       l   Module 1
              ¡ Introduction and Overview

              ¡   Correction vs. Corrective Action
                      n Understanding of all elements of CAPA process
                        step as required by ISO and regulatory agencies
                      n Introduction to CAPA elements in a practical and

                         proven manner which can be immediately applied
                         in your organization
                     n   Supporting stories and practical examples of CAPA
                         - when each is appropriate and when one or the
                         other is not appropriate
                     n   The regulations and international requirements
                         for CAPA and the clear understanding how to suit
                         your procedures, work instructions and forms to
                     address it
       l   Module 2
                                                                                    
              ¡ Examples of problem solving tools, management tools

                  and measurement tools, which are great for
                  identification of the true root cause(s) of the issue
              ¡   These tools also used for corrective actions, for most
                  optimal definition of the improvement, for preventive
                  actions
              ¡   Visual representation of the tools and examples where
                  and when to use them
              ¡   Importance of proper assignment of a CAPA
              ¡   Examples are provided when it might be a good thing to
                  assign a CAPA to a team
              ¡   Examples when would be a good thing to assign a CAPA
                  to an individual
              ¡   Examples and definitions of teams and team members
                  roles and responsibilities
              ¡   It can be used and applied in other areas inside and/or
                outside the organization when and where team work is
                required and expected
            ¡   This section by itself can be taken out and applied to
                other processes and practices within or outside of the
              organization with the goal of continuous improvement
     l   Module 3
            ¡ Emphasize the importance and need of completing the
              verifications and/or validations of the actions taken to
                ensure that the issue has been resolved and the true
                root cause of the issue has been removed
            ¡   Real-life examples and suggestions which can be used
                immediately after completing the webinar
     l   Module 4
            ¡ Examples how to appropriately award and recognize
              teams and individuals for producing the results
            ¡ Additional references and pointers where more

                successful examples and instructions can be found so
                that you and your organization can benefit and profit
                more from the CAPA process and CAPA teams - and
                maybe more importantly have those outside the quality
                department more engaged and interested in
                participating in CAPA and continuous improvements
     l   Q&A


 Click here to register for this webinar


  Who Will Benefit:


     l   Quality Managers
     l   Quality Engineers
     l   Small business owners
     l   CAPA investigators
     l   Inspectors
     l   Six Sigma specialists
     l   Consultants



It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely
benefit from this program.

For more information, please contact the event coordinator. We look forward to seeing you at the webinar.

Best regards,
Event-coordinator
GlobalCompliancePanel



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DOCUMENT INFO
Description: This CAPA training program helps you to understand, in 10 easy steps, the entire CAPA process. It includes elements of Quality Tools, Team Effectiveness, Awards & Recognitions, and Verification & Validation of actions taken. Attend this webinar to grasp the A to Z of CAPA and learn how to implement & manage it for success.