- TypeWebinar
- Location Denver, Colorado, United States
- Date 16-01-2018
Education/Teaching/Training/Development
Business Development
Manufacturing
Food Processing
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
LEARNING OBJECTIVES
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: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Learn about FDA deviation investigations and root cause analysis in this informative webinar, along with the ways of resolving the deviations.