Introduction to Corrective & Preventive Action - CAPA
Why CAPA
Applicable Regulation & Standards
Root Cause Determination
When does a deficiency require CAPA?
CAPA Tools & Methodology
Actions to Prevent Recurrence
Introduction to Industrial Sterilization
Radiation Sterilization & Validation
EO sterilization and Validation
Contract Sterilization
Workshop
Utilizing CAPA tools to solve typical quality deficiencies
Utilizing CAPA tools to solve sterilization deficiencies
Instructors will lead attendees through several ‘real case’ exercises related to CAPA and sterilization & quality deficiencies; attendees will present findings to the rest of the group
Who should Attend
Personnel in Medical Device Manufacturing and Sterilization facilities, including CAPA Team Members, QA Personnel, Quality Engineers, SA Personnel, Anyone with direct hands on experience with sterilization & troubleshooting and Operations Managers.
Past Events
2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action 2012 - 14-15 Jun 2012, Hotel Irvine, California, United States (30084)
Please, check "2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action" official website for possible changes, before making any traveling arrangements
