GMP Complaint Systems, Adverse Event Reporting and Product Recalls 2017
09 Feb 2017
Webinar
Description
Topics
GMP standards for an effective recall system
GMP requirements for complaint documentation and management
To understand the specific requirements for organization, procedures and resources
To identify the key issues in product complaint and recall handling
To understand and develop actions to resolve current issues applicable to you
Who should Attend
Regulatory Compliance Professionals
Those working in the FDA compliant industries such as pharma, medical devices and biotech
Quality Control Professionals
Quality Assurance Professionals
Complaint Handling Professionals
Regulatory Affairs Professionals
Service Technicians and Engineers
Quality Engineers
Process Development Personnel
Manufacturing and Design Engineers
Past Events
GMP Complaint Systems, Adverse Event Reporting and Product Recalls 2017 - 09 Feb 2017, Webinar (65354)
Important
Please, check "GMP Complaint Systems, Adverse Event Reporting and Product Recalls" official website for possible changes, before making any traveling arrangements
