Corrective and Preventive Action (CAPA) and Complaint Handling in Medical Device.2015

Topics

• CAPAs and complaints are key focus areas having GMP guidelines and this webinar will review the ins and outs of how to manage these systems and effectively address questions FDA will likely raise during inspections

Who should Attend

• Directors in Quality Assurance
• VP’s in Quality Assurance
• Quality Professionals
• Quality Managers
• Small Business Owners