Bullet-Proof CAPA

Live Webinar on

Bullet-Proof CAPA


Course "Bullet-Proof CAPA" has been pre-approved by RAPS as
eligible for up to 1.25 credits towards a participant's RAC

Register Now

recertification upon full completion.
Date & Time:
Instructor Profile:
Thursday, July 26, 2012
10:00 AM PDT | 01:00 PM EDT
Duration: 75 Minutes
Instructor: Jasmin NUHIC
Jasmin NUHIC
Sr. Compliance Quality
Location: Online
Price : $245.00 (for one participant)
Engineer, Medtronic
Jasmin NUHIC serves a major
Overview:
medical devices OEM as a Sr.
This CAPA training program helps you to understand, in 10 easy
Compliance Quality Engineer and 21
steps, the entire CAPA process. It includes elements of Quality Tools,
CFR Part 11 Subject Matter Expert.
Team Effectiveness, Awards & Recognitions, and Verification &
He also served ASQ section as a
Validation of actions taken. Attend this webinar to grasp the A to Z of
chair for two consecutive terms, has
taught quality certification exam
CAPA and learn how to implement & manage it for success.
prep course, completed numerous
software validations and obtained
Why Should You Attend:
over 25 different certifications in
leadership, quality, software
We have found out, through auditing many organizations world-wide
validations, and more. Jasmin NUHIC
that the organizations are pretty good when it comes to corrective
has conducted Webinars on this and
actions yet they are not nearly as good when it comes to the
other topics with high attendance
preventive actions. This webinar should provide you with enough
and appreciation. ...more
ideas, suggestions and HOW TOs that you and your teams and
organization overall get much better on the preventive actions and
even better on the corrective actions. Includes all elements of CAPA
Suggest a Topic
More Webinars
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
About GlobalCompliancePanel
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online
compliance training by creating a single window of learning opportunities for compliance professionals & providing a
forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our
commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training
sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions,
giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs.
GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning
and development on/through our website. Keep track of all webinars arranged for your industry through notifications &
event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for
professionals.
GlobalCompliancePanel
www.globalcompliancepanel.com
1000 N West Street Suite,
1200 Wilmington DE 19801
Phone: 800-447-9407 or
Fax your PO to: 302-288-6884
If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe

---