Material Receiving & Storage According to GMP Requirements

Outline

• Introduction to GMP and warehouse compliance requirements
• Types of materials and storage specifications in the pharmaceutical industry
• Material receiving procedures: verification, inspection, sampling & decision-making
• Documentation, records, and required receiving forms
• Material coding, labeling, and traceability systems
• FIFO / FEFO / Batch Control
• Environmental monitoring and storage conditions (temperature – humidity – ventilation)
• Warehouse layout and designated storage zones
  (Approved / Quarantine / Rejected / Returned / Sampling Area)
• Handling hazardous and sensitive materials
• Safety & security requirements in warehouse operations
• Common non-conformities during inspections and how to avoid them
• Internal audit requirements and readiness for regulatory inspections

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