Goods-in Inspection and Transport Damage Form
Goods-in forms and damage reports.
900 Skr
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Purpose:
Provides standardised forms to document goods-in inspections and the identification, assessment, and recording of transport-related damage to medicinal products or materials upon receipt.
Regulatory Alignment:
Aligned with EU GDP requirements for receipt, inspection, and handling of medicinal products, with relevant interfaces to EU GMP expectations for material control and quality system documentation.
Included Files:
• Goods-in inspection form
• Transport damage reporting form
• Receipt verification and follow-up documentation fields
Format:
Microsoft Word or Microsoft Excel (fully editable)
Intended Users:
Wholesale distributors, pharmaceutical manufacturers, quality assurance teams, warehouse, and logistics personnel involved in receipt and inspection activities under EU GDP and EU GMP.