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10 Steps to Success of Effective Corrective And Preventive Actions (CAPA)

 
  August 22, 2012  
     
 
ComplianceOnline, Online Event
2012-09-25


Why Should You Attend:

Organizations are pretty good when it comes to corrective actions, yet they are not nearly as good when it comes to the preventive actions. This webinar will provide you with enough ideas, suggestions and HOW TOs that you, your team and the organization overall get much better on the preventive actions and even better on the corrective actions. We will discuss all the elements of CAPA process steps as required by ISO and regulatory agencies. In addition, it is represented in a practical and proven manner which can be immediately applied in your organization.

This course provides simple, easy-to-follow steps from identification of an issue or identification of an opportunity for improvement all the way to the end of the process and harvest of the benefits. The presentation is structured in a way that can easily be converted into a Standard Procedure/Policy for CAPA and/or into effective Work Instructions. In addition to the CAPA process, this webinar includes elements of quality tools, team effectiveness, awards and recognitions, verifications and validations of actions taken and much more. This webinar will not only provides you with more information on CAPA but also provides you with HOW TOs to make your CAPA more effective and successful.

Areas Covered in the Seminar:

  • CAPA Process Steps include all elements.
  • Quality Tools For Problem Identification and Definition.
  • Verification and Validations of Actions Taken.
  • CAPA Ownership and Assignment.
  • Corrections versus Corrective Actions.
  • Closure and Recognitions.
  • Continuous Improvement.
Event Details:
 
Date:                    September 25, 2012
Time:                    09:00 AM-11:00 AM PDT
Cost:                    $299 per attendee per computer terminal
Registration:        SIgn-Up on-line now.  Add to your shopping cart.
 
 
Organized by: ComplianceOnline
Invited Speakers: Jasmin NUHIC - Professional with proven record of leading teams that deliver projects in full scope, below a budget and ahead of schedule through process optimization, business growth and talent development. Over 12 years of experience in FDA regulated industry with vast experience in operations, quality management systems, manufacturing, concurrent engineering, program management and information systems. Positive and verifiable track record in continuous improvement and cost saving initiatives through use of lean sigma and six sigma methodologies.

Salim Khan - holds a master degree in Manufacturing Engineering, an MBA and BS in Mechanical Engineering. He is also ASQ certified Six Sigma Black Belt, Certified Reliability Engineer, Certified Quality Engineer. Salim has successfully implemented several design control and risk management processes for medical device companies. He also has extensive experience in developing efficient product development process. He enjoys statistics and has completed several process validations.
 
Deadline for Abstracts: 2012-09-25
 
Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702436?channel=hummolgen
E-mail: referral@complianceonline.com
 
   
 
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