Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices

Posted By : User Ref No: WURUR40208 0
  • Image
  • TypeWebinar
  • Image
  • Location Newark, Delaware, United States
  • Price
  • Date 22-08-2019
Root  Cause Analysis for CAPA - Myths, Challenges, and Best Practices, Newark, Delaware, United States
Webinar Title
Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
Event Type
Webinar
Webinar Date
22-08-2019
Last Date for Applying
22-08-2019
Location
Newark, Delaware, United States
Organize and Presented By
247compliance
Sponsored By
247compliance
Organizing/Related Departments
Food and Drug Administration
Organization Type
Event Organizing Company
WebinarCategory
Non Technical
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Chemical

Food Processing

Location
Newark, Delaware, United States
  • OVERVIEW

This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process.  We’ll also cover the essentials of doing a failure investigation.

  • LEARNING OBJECTIVES

 

  • Build the right team
  • Develop a problem statement
  • Failure Investigation
  • Data Collection
  • Analysis Tools and Techniques
  • How tVerify your Results
  • Real Lessons Learned
  • Do’s and Don’ts of CAPA
  • Best Practices
  • Inspection Readiness
     
  • WHY SHOULD YOU ATTEND

CAPA is the cornerstone of quality improvement and it depends on an effective root cause analysis. Conducting an effective root cause analysis (RCA) can be a daunting task. And without a good root cause analysis, your CAPA will not result in the desired improvement. You will waste precious time and money and still end up with unsatisfactory results. This webinar will give you insights and lessons learned from a certified Master Black Belt and industry expert with over 30 years’ experience. You will learn about the RCA toolbox and how to get permanent resolution to your significant quality problems.

  • WHO WILL BENEFIT?

 

  • Quality Engineers
  • Manufacturing Engineers
  • Process Engineers
  • Compliance Specialists
  • Auditors
  • CAPA Specialists
  • CAPA Project Leaders
  • CAPA Managers
     
Registration Fees
Available
Registration Fees Details
Live session for 1 participant $199 Live + Recorded Session $269 Live + Transcript $249 Live + Training CD Free shipment within 72 hours from the date of webinar completion. $450 On Demand Options Transcript $179 Downloadable recorded session $239 Training CD Free shipment within 72 Hours, from the date of webinar completion $350 Group Session unlimited participants + Recorded $799
Registration Ways
Email
Phone
Website
Other
Address/Venue
  247compliance 2035 Sunset Lake, RoadSuite B-2, Newark, Delaware - 247compliance  Pin/Zip Code : 247compliance
Official Email ID
Contact