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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

Brownfield Facility Assessment

Home » Brownfield Facility Assessment
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Brownfield Facility Assessment (Existing Plant)

For existing pharmaceutical facilities (Brownfield projects), our experts perform a detailed review of the current plant layout and engineering systems to identify compliance gaps with regulatory standards.

Our support includes:

  • Review of facility layout and building design to ensure compliance with GMP requirements.
  • Guidance for renovation, modification, and facility upgrades to improve regulatory compliance.
  • Evaluation of pressure zoning layout to maintain proper airflow and contamination control between different areas.
  • Review of cleanroom classification and area segregation according to product risk and manufacturing processes.
  • Assessment of man and material movement flow to avoid cross-contamination and ensure proper personnel and material pathways.

Based on the assessment, our team provides practical recommendations and engineering guidance for facility improvement and regulatory compliance.

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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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