2020 - FDA Recalls - Before You Start, and After You Finish
Date2020-10-08 - 2020-10-09
Deadline2020-09-29
VenueWashington, D.C, USA - United States
KeywordsFDA Recall; FDA recall guidance; Regulatory management
Topics/Call fo Papers
FDA's recall authority and program launches you into a project of crisis management. You will learn how to establish a roadmap for conducting recalls. The knowledge you gain will sharpen your recall management decisions and strategy. You will learn how to use the FDA's health risk criteria so you can develop effective recall procedures. One critical aspect of recalls involves the identification of the root cause of the recall and how you could or should prevent that problem from happening again. Your corrective and preventive action program (CAPA) and quality assurance functions require a rigorous approach to prevent a chronic history of recalls. Reiterative recalls lead the FDA to the conclusion that, "You don't get it."
Other CFPs
- The Drug Development Process from Concept to Market
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
- Analytical Instrument Qualification and System Validation
- Laboratory Inspection and Auditing
Last modified: 2020-04-04 00:35:36