Corrective and Preventive Action (CAPA) Training
Training Duration: 2 days
This course covers the basic concepts for implementing and maintaining a corrective and preventive action (CAPA) program. In addition to understanding why a CAPA program is needed, tools and techniques are provided on how to operate a CAPA program. This course should be mandatory for any person in QA who handles CAPAs and those in other departments who perform investigations and CAPAs.
Training Features
- Day one consists of CAPA concepts, requirements and processes.
- Day two consists of training on how to write CAPA reports and perform root cause analysis.
- When possible we use case studies from you own CAPA files in order to make the workshop more relevant.
- Content focuses on the medical devices and pharmaceutical common validation practices per federal regulation.
- How to effectible comply with FDA expectations regarding the CAPA process.
- Information on what to expect during FDA GMP inspections.
Training Benefits
- Employees will have and increase knowledge of how effectively comply with the CAPA process.
- Increase CAPA technical writing.
- Employee increase performance, less mistakes due to lack of basic understanding of the CAPA regulations.
International Quality Consulting bring a diverse team of consultants to our clients. We are constantly expanding our roster of internationally recognized associates. Our trainers and consultants average over 30 years experience in the FDA regulated environment – many of which are ex-FDA. Our associates bring a wealth of experience to help meet your consulting and training needs.