How to Avoid an FDA Warning Letter with a Strong CAPA Program 2015
04 Mar 2015
Webinar
Description
Topics
Common areas of the quality system where critical mistakes are made
The FDAs requirement for a strong quality system and key focus points for improvement
How to identify timely and accurate Corrective and Preventive Actions(CAPA) within the quality system
Your role and the FDAs requirements and expectations during a quality inspection
Tips and techniques for investigating and documenting non-conformances
Who should Attend
Investigators
Engineers
Manufacturing Supervisors
QA/QC Professionals
Technicians
Past Events
How to Avoid an FDA Warning Letter with a Strong CAPA Program 2015 - 04 Mar 2015, Webinar (49192)
Important
Please, check "How to Avoid an FDA Warning Letter with a Strong CAPA Program" official website for possible changes, before making any traveling arrangements
