FDA’s Adverse Event Reporting and Product Recalls

The FDA’s Adverse Event Reporting and Product Recalls 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 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

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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