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aimintellixglobalaimintellixglobal
  • Home
  • About Us
  • Services
    • Gxp Audit
      • GMP Audit
      • GDP Audit
      • GLP Audit
    • Quality Compliance Services
      • QMS
      • Audit and Inspection Readiness
      • Qualification and Validation
    • Regulatory Affairs
      • Submissions & Publishing
      • Artwork & Labelling
      • Regulatory Intelligence
      • Product Life Cycle Maintenance Support
      • End-to-End Support
    • Pharmaceutical Engineering Services
      • Brownfield Facility Assessment
      • Greenfield Project Support
      • FAT Audit Support
  • Industries
    • Pharmaceutical
      • Raw Material
        • API
        • Excipient
      • Finished Product
        • OSD (Tablet/Capsule)
        • Biological
        • Liquid formulation
    • Biological
    • Education
      • Sanskrit Language
      • Vedic Science
      • Mind Wellness
      • Pharmacy
  • Training
    • All programs
    • Career Development
    • For Working Professionals
    • For Freshers
    • Latest Courses
  • Contact

FAT Audit Support

Home » FAT Audit Support
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FAT (Factory Acceptance Test) Audit Support

Our team also provides Factory Acceptance Test (FAT) audit support for pharmaceutical manufacturing equipment before installation at the facility.

Our FAT services include:

  • Guidance on how to plan and conduct FAT audits according to regulatory expectations.
  • Review of equipment design, functionality, and compliance with user requirement specifications (URS).
  • Verification of equipment performance, safety features, and control systems.
  • Review of documentation such as test protocols, calibration certificates, and technical manuals.
  • Identification of any technical or compliance gaps before equipment shipment to the manufacturing site.

This process helps ensure that equipment meets quality, safety, and regulatory standards before installation and qualification.

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AIM INTELLIX GLOBAL SERVICE Pvt. Ltd. provides end-to-end consultancy and implementation support for EU-GMP compliance across pharmaceutical facilities, including Injectables, OSD, and allied dosage forms.

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