How to Avoid an FDA Warning Letter with a Strong CAPA Program 2015 is a webinar that covers topics such as:
- 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
How to Avoid an FDA Warning Letter with a Strong CAPA Program 2015 is intended for:
- Investigators
- Engineers
- Manufacturing Supervisors
- QA/QC Professionals
- Technicians
