🎤  Alan M. Golden         |  ðŸ“…  October 22, 2024   |  ðŸ•’  11 AM Eastern Time US





Description:

Corrective Actions/Preventive Actions are an integral part of a robust quality system in both pharmaceutical and medical device manufacturing. The ability to be able to determine the root cause of a product or manufacturing issue and put effective corrections in place is critical to continued product quality. Understanding the process of root cause investigations and the appropriate corrective actions/preventive actions will help ensure continued product quality.

CAPA is a required part of both pharma and medical device quality systems. An understanding of the CAPA system and putting into place a robust process will help ensure quality products and smooth manufacturing.


Areas Covered in the Session :

  • Gain an understanding of the CAPA process
  • Understand the need for CAPA
  • Discuss inputs into the CAPA process
  • How to put a good process in place

Who Should Attend: 

  • Quality Assurance Departments
  • Quality Control Departments
  • Regulatory Affairs Departments
  • Research and Development Departments
  • Manufacturing Departments
  • Engineering Departments



Read more