CAPA Details, Implementation and Q&A in Medical Device Setting  
Date
Mon, Dec 05, 2011 at 9:00 am to 11:00 am PST
Palo Alto, CA
Date, Time and Location
Starting
Mon, Dec 05, 2011 at 9:00 AM PST
Ending
Mon, Dec 05, 2011 at 11:00 AM PST
Location & Address
Online Event
2600 E. Bayshore Road
Palo Alto, CA
United States-94303

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Ticket Types Price
($)    
  Fee 
($)    
  Qty
Online Training  (more) 299.00 5.98 USD 1 38788 299.00 5.98 Online Training N/A 1
Sale Ended
Mon, Dec 05, 2011 at 9:00 am to 11:00 am
  
Event Details
This 2-hr Medical Device CAPA training will cover key CAPA process skills such as identifying non-conformances, root cause analysis, and steps to implement CAPA and check its effectiveness in a Medical Device setting.
This course will not only focus on CAPA, but on how to conduct investigations including non-conformances, customer complaints, out of specifications, or any other investigations you may face within your organization.

Learning Objectives:

By participating in this workshop, attendees can improve their ability to:

  • Gather relevant information on problems through specific, focused questioning.
  • Pinpoint root causes using facts instead of guesswork or opinion.
  • Avoid costly experiments and trial fixes by logically testing possible causes.
  • Assess and prioritize each nonconformance based on risk.
  • Target potential problems before they happen and develop actions to prevent them.
  • Check effectiveness of corrective actions.
  • Document the analysis in an easy-to-use format.
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Event Hosted By
ComplianceOnline
ComplianceOnline, we are focused on :
Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.
Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.
Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.
Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.
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