The GMP Complaint Systems, Adverse Event Reporting and Product Recalls 2017 is a webinar that covers topics such as:
- 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
The GMP Complaint Systems, Adverse Event Reporting and Product Recalls 2017 is intended for:
- 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