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WorldConference

Root Cause Analysis: Foundation of Investigations and CAPA

Root Cause Analysis

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Who should attend?

Quality Managers Auditors Operations and Manufacturing Personnel Validation Engineers Product/Process Development Principal Investigators, Site Research Directors and Coordinators Quality Assurance Staff Regulatory Managers and Professionals Compliance Managers and Professionals

Details

Overview:

Why you should attend:

  • What do the regulations say?
  • Four Phases of RCA
  • Promote the ability to provide problem-solving support in situations where one is not an expert in the process or technology involved
  • Expand the range of tools available for analysis of problem situations
  • Apply a variety of tools to narrow down the possible causes of a problem
  • Learn how to investigate serious and complex incidents and events
  • Learn the importance of near-miss investigations, incident classification, and data trending
  • Learn how to identify root causes (not just causal factors) using proven techniques
  • A robust investigation and root cause analysis process, as well as, basic root cause analysis tools that can transfer to any company
  • Understanding of the major cause categories that can affect your processes - and which categories tend to be the most overused and underused
  • How to identify whether you’re finding the direct or the root cause of a problem
  • The ability to identify the true cause of an issue and, as a result, identify and implement more effective CAPAs
  • Tips for implementing a root cause analysis training program at your facility - and what support is required for the process to work once people are trained
  • Apply performance management concepts in case studies with a focus on prevention and issues management
  • Recognize components of effective corrective action planning and documentation
  • Identify examples of corrective action planning for different site noncompliance case scenarios
  • Discuss successful preventive action planning and implementation
  • Develop, establish, implement, and maintain effective root cause analysis and CAPA procedures and other documentation
  • Discussions on proper CAPA system maintenance, documentation of the Corrective and Preventative Actions and developing a robust CAPA plan
  • Attendees are encouraged to bring examples of their work from the functional area on the various topics as applicable for group discussion
  • Challenges and possible solutions will be discussed, and examples will demonstrate how the requirements can be put into practice
  • Review and discuss pain points, challenges and solutions
  • Are you in compliance with the FDA Corrective and Preventive Action (CAPA) requirements?
  • Do you know how to identify root cause and how to close out your investigation?
  • Understand that the cost of regulatory noncompliance remediation is significantly greater than the cost of compliance
  • Leave the seminar with a better understanding of structured root cause analysis, effective investigational techniques and ensuring that the CAPA system is well established and maintained

Speaker

David R. Dills

Global Regulatory Affairs & Compliance Consultant and President, NovaQual 

Location:  Philadelphia Date: May 16th & 17th, 2018 and Time: 9:00 AM to 5:00 PM

Venue:  WILL BE ANNOUNCED SOON

Price:

Price: $1,295.00 (Seminar Fee for One Delegate)

Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)*

 Register now and save $200. (Early Bird)

Until April 20, Early Bird Price: $1,295.00 From April 21 to May 14, Regular Price: $1,495.00

Sponsorship Program benefits for “Root Cause Analysis: Foundation of Investigations and CAPA” seminar

For More Information- https://www.globalcompliancepanel.com/control/sponsorship 

Contact us today!

NetZealous LLC DBA GlobalCompliancePanel

john.robinson@globalcompliancepanel.com  

support@globalcompliancepanel.com 

Toll free: +1-800-447-9407

Phone: +1-510-584-9661

 Website: http://www.globalcompliancepanel.com

 

Registration Link - https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901735SEMINAR?SEO

Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/

Like us our Facebook page: https://www.facebook.com/TrainingsAtGlobalCompliancePanel/

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Prices

Price: $1,295.00 (Seminar Fee for One Delegate) Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)* Register for 10 attendees Price: $7,122.00 $12,950.00 You Save: $5,828.00 (45%)* Register now and save $200. (Early Bird) Until April 20, Early Bird Price: $1,295.00 From April 21 to May 14, Regular Price: $1,495.00

Contact

John Robinson
support@globalcompliancepanel.com

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