Investigating Deviations Webinar,Investigating Deviations Online Webinar,Webinar on Investigating Deviations,Best Practices for Investigating Deviations Webinar,Best Practices for Investigating Deviations

Best Practices for Investigating Deviations - online live webinar on January 2018 by Training Doyens

Webinar Information


Best Practices for Investigating Deviations


Best Practices for Investigating Deviations, Denver, Colorado, United States
Webinar Title
Best Practices for Investigating Deviations
Event Type
Webinar
Webinar Date
16-01-2018
Last Date for Applying
16-01-2018
Location
Denver, Colorado, United States

Publish / Maintain / Marketing / Hosted By
Organization Name / Organize By
Training Doyens
Organizing/Related Departments
Training Doyens
Organization Type
Organization/Company
Webinar Category
Both (Technical & Non Technical)
Webinar Level
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Business Development

Manufacturing

Food Processing

Location
Denver, Colorado, United States

OVERVIEW

Deviation investigations are a very common topic to be reviewed during FDA investigations. Ensuring the firm has robust and complete write-ups of these situations is key to a successful audit. Having inadequate investigations could potentially cause some severe issues for the company and may sometimes result in warning letters, consent decrees or recalls.

WHY SHOULD YOU ATTEND

Proper root cause analysis of the issue is necessary to make sure that the firm is focusing on the real problem and subsequently the proper corrective and preventative actions can begin.

This webinar will help attendees understand how to use root cause analysis tools and CAPA plans to successfully resolve deviations and non-conformances.

AREAS COVERED

  • Review of FDA and Regulatory Requirements for Investigations
  • What is the definition of a Deviation?
  • Types of Deviations/Identification of Deviations
  • Conducting the Investigation
  • Interviews – dos and don’ts
  • Source Documents/Evidence
  • Determining Root Cause and Effective/Sustainable CAPA to avoid 483 observations

LEARNING OBJECTIVES

  • Discuss what to do when problems occur
  • Outline the requirements of the Deviation and procedure including the deviation report
  • Choose the most appropriate Root Cause Analysis methods for the situation
  • Discuss how to conduct the deviation and the tools to be used in the process
  • Review and discuss an example deviation using the tools suggested

WHO WILL BENEFIT

Quality Assurance/Quality Control Directors, Managers, and Specialists

Regulatory Affairs/Regulatory Compliance Directors, Managers, and Specialists

Engineering/Development Directors, Managers, and Specialists

Email: support@trainingdoyens.com

Toll Free: +1-888-300-8494

Tel: +1-720-996-1616

Fax: +1-888-909-1882

Others Details

Learn about FDA deviation investigations and root cause analysis in this informative webinar, along with the ways of resolving the deviations.

Registration Fees
Available
Registration Fees Details
Live Session for one participant $199 Corporate Live Session Group – Max 10 Participants from one location. $549 Recorded Session Get unlimited access to audio recording of the webinar for 6 months. $219 Training CD MP3 files, PDF presentation and reference manual will be delivered on a CD $399 Super Combo Offer 1 Live and Recorded webinar $329 Super Combo Offer 2 Live and Training CD $499
Registration Ways
Email
Phone
Website
Other
Address/Venue
Online Webinar 
Official Email ID
support@trainingdoyens.com
Contact
Training Doyens

26468 E Walker Dr, Aurora, Colorado 80016-6104

support@trainingdoyens.com

   7209961616