GMP change management: Jumping on the fast track from deviation to resolution

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Fix your slow change control process 

Using a real-world use case involving a deviation in a pharmaceutical product's repackaging process we'll demonstrate how Scilife’s eQMS can help you maintain compliance, ensure traceability, and optimize your change management workflows.

What you’ll learn in this session:

• Manage a change request triggered by a deviation and the subsequent CAPA.
• Navigate the complete change request workflow from start to finish.
• Create, assign, and complete tasks within the change plan.
• Ensure compliance with 21 CFR Part 11 through electronic signatures. 
• Leverage Scilife's KPIs tool for valuable insights into your change control performance.
  
  

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