Root Cause Analysis and Tools

Instructor: John E Lincoln
Product ID: 700812
  • Duration: 60 Min

recorded version

1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Apr-2008

Training CD / USB Drive

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Read Frequently Asked Questions

One of the 4 major areas for FDA-regulated companies’ product compliance is CAPA (Corrective and Preventive Action).


Root cause analysis is inherent in Hazard Analysis / Product Risk Management under ISO 14971, a component of any viable lean 6-sigma program, and makes for good business.

Both CAPA, all associated complaint handling and adverse events / MDR reporting systems require the ability to dissect a problem and get down to the root cause, in order to handle product correction, impact analysis, corrective action, and preventive action. Root cause analysis is therefore fundamental to addressing and solving problems, as well as developing methods to prevent their (and other related problems) recurrence. Root cause analysis is inherent in Hazard Analysis / Product Risk Management under ISO 14971, a component of any viable lean 6-sigma program, and makes for good business.

Areas Covered in the seminar:

  • Developing and using the Investigation Template.
  • 4 basic steps to problem solving.
  • 7 basic and simple tools - powerful tools.
  • Tools for investigation.
  • Tools for problem solving.
  • Validate.
  • Monitor.
  • After the "real" root cause(s) is identified - Now what?
  • When to "jump out of the process"?

Who will benefit:

  • Management at all levels.
  • Project Leaders.
  • Regulatory Affairs.
  • Quality Systems Personnel.
  • R&D and Engineering Staff.
  • All charged with new product development, risk analysis / management, regulatory submissions, initiating / overseeing company-wide training, production, validation, and complaint handling.
  • Identified staff, operations and line personnel who desire to assume "train-the-trainer" roles to train teams in problem / OOS reduction.

Instructor Profile:

John E. Lincoln, Consultant, has successfully developed and implemented and trained to device, pharma, medical gases, and dietary supplements CGMP-compliant systems. He has conducted compliance audits in all these areas. His systems have passed FDA audit or submission scrutiny, and have been described in peer-reviewed technical articles, and workshops, world wide. John has also managed pilot production, regulatory affairs, product development projects; with over 25 years of experience, in FDA-regulated industry - working with start-ups to Fortune 100 companies, including Abbott Laboratories, Hospira, Tyco / Mallinckrodt. John serves on the Reader and Editorial Review Boards of MDDI Magazine and the Journal of cGMP Compliance, and Intermountain Biomedical Association); he publishes a newsletter. He is a graduate of UCLA.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

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Product Reviews Write review

Excellent presenter
- Anonymous

Really enjoyed Mr. Lincoln's presentation, his delivery, his expert knowledge, and his relaxed yet throughly engaged manner. You can tell he has lived all of this for a very long time. I look forward to purchasing more Web Seminars from Mr. Lincoln through ComplianceOnline. Our RA/QA Director, Mr. Al Parrotta, recommended this Web Seminar as he has had experience with both Mr. Lincoln and ComplianceOnline. Thank you Mr. Lincoln for the wonderful information and presentation!
- Anonymous

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