Developing an Effective CAPA Program for GMP Operations 2015 covers topics such as:
- Roles and responsibilities of manufacturers
- Hy an effective CAPA system is important
- Determining root causes
- Identifying sources of infractions
- CAPA Tracking System and documentation
Developing an Effective CAPA Program for GMP Operations 2015 brings together:
- Quality Assurance scientists
- Laboratory Analysts
- QA/QC Managers
- QA/QC Analysts
- Inspectors
- Auditors
- Manufacturers of raw materials and excipients
- Pharmaceutical development and manufacturing personnel
- Contract laboratory Organization personnel
