Streamlining Your Internal Auditing Process
June 24, 2019· Ended
Conference
Palo Alto, United States
In Person
Deadline: June 22, 2019
About This Event
This webinar will cover creating of a value-added internal auditing program that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485. It will include how to set up and manage the auditing system as well as how to conduct an internal audit and document the results and any nonconformities. It will discuss the value of a good internal auditing program.