The Downtime in the Pharmaceutical Industry

Has there been downtime period in your facility?

What are impacts and how risk assessment approach can help you to stay in state of control?

Agon will help you to assess all deviations during the downtime in all GMP systems, prepare the required risk assessment studies and issue a comprehensive CAPA to cover all gaps occurred in the downtime.

The following Departments are considered:

  • QC Department
  • Engineering Department
  • Production Department
  • Warehouse Department
  • QA Department
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