Avoiding FDA Form 483: Streamlining supplier qualification with Scilife

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Maintain a fully compliant supplier management program 

In this free session, we'll demonstrate how Scilife’s eQMS simplifies supplier qualification by automating key processes, ensuring compliance with FDA regulations, and reducing the risk of costly 483 findings. 

What you’ll learn in this session:

• Efficiently create and manage supplier questionnaires within Scilife.
• Perform robust quality assessments based on supplier data. 
• Use Scilife's tagging system to categorize suppliers based on risk.
• Document every step of the supplier qualification process.
  
  
  

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