The FDA s Adverse Event Reporting and Product Recalls 2018 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
- Best practices related to documentation, management and regulatory reporting
- How the FDA responds to adverse event reports and the regulatory consequences for not reporting
- To understand and develop actions to resolve current issues applicable to you
The FDA s Adverse Event Reporting and Product Recalls 2018 is intended for:
- Quality Control Departments
- Quality Assurance Departments
- Compliance Departments
- Regulatory Affairs Departments
- Complaint Handling Professionals
- Manufacturing Departments
- Production Departments
- Engineering Departments
- Operations Departments
- Service Technicians
- Process Development Professionals
- Design Assurance Teams
