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SOP Guide for Pharma

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SOP for Shipment Verification

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Shipment Verification Procedure

Purpose

The purpose of this SOP is to establish procedures for verifying the accuracy of incoming and outgoing shipments in the pharmaceutical warehouse to ensure the quality, integrity, and compliance of products.

Scope

This SOP applies to all personnel involved in the shipment verification process within the warehouse.

Responsibilities

  • Warehouse Manager: Overall responsibility for implementing shipment verification procedures and ensuring compliance.
  • Receiving Staff: Responsible for verifying incoming shipments against purchase orders and shipment documentation.
  • Shipping Staff: Responsible for verifying outgoing shipments against sales orders and packing lists.
  • Quality Assurance: Responsible for verifying the quality and compliance of products during shipment verification.
See also  SOP forĀ  Cleaning of Warehouse

Procedure

  1. Incoming Shipments:
    • Receive incoming shipments and compare them against the corresponding purchase orders.
    • Inspect incoming shipments for damage, discrepancies, or deviations from specifications.
    • Verify the accuracy of quantities received and reconcile any discrepancies with suppliers.
  2. Outgoing Shipments:
    • Review sales orders and packing lists to ensure accuracy and completeness of outgoing shipments.
    • Select appropriate packaging materials and ensure products are securely packed for transit.
    • Verify that all required documentation, including shipping labels and invoices, is included with the shipment.
  3. Quality Verification:
    • Conduct quality checks on incoming and outgoing shipments to verify product integrity and compliance.
    • Inspect products for damage, defects, or signs of tampering.
    • Verify product expiration dates, lot numbers, and other critical information against specifications.
  4. Documentation:
    • Maintain accurate records
of shipment verification activities, including inspection results and any corrective actions taken.
  • Document any discrepancies or non-conformances identified during the verification process.
  • Ensure that all shipment documentation is properly filed and archived for future reference.
  • Abbreviations

    • SOP: Standard Operating Procedure

    Documents

    • Shipment Verification Log
    • Quality Inspection Reports
    • Corrective Action Reports

    SOP Version

    Version 1.0

    See also  SOP for MSDS
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    Standard Operating Procedures V 1.0

    • Aerosols
    • Analytical Method Development
    • Bioequivalence Bioavailability Study
    • Capsule Formulation
    • Clinical Studies
    • Creams
    • Data Integrity
    • Dental Dosage Forms
    • Drug Discovery
    • Environment, Health and Safety
    • Formulation Development
    • Gels
    • Good Distribution Practice
    • Good Warehousing Practices
    • In-Process Control
    • Injectables
    • Liquid Orals
    • Liposome and Emulsion Formulations
    • Lotions
    • Lyophilized Products
    • Maintenance Dept.
    • Medical Devices
    • Metered-Dose Inhaler
    • Microbiology Testing
    • Nanoparticle Formulation
    • Nasal Spray Formulations
    • Nebulizers
    • Ocular (Eye) Dosage Forms
    • Ointments
    • Otic (Ear) Dosage Forms
    • Pharmacovigilance
    • Powder & Granules
    • Purchase Departments
    • Quality Assurance
    • Quality Control
    • Raw Material Stores
    • Regulatory Affairs
    • Tablet Manufacturing
    • Rectal Dosage Forms
    • Transdermal Patches
    • Vaginal Dosage Forms
    • Validations and Qualifications

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    NEW! Revised SOPs – V 2.0

    • Aerosols V 2.0
    • Analytical Method Development V 2.0
    • API Manufacturing V 2.0
    • BA-BE Studies V 2.0
    • Biosimilars V 2.0
    • Capsules V 2.0
    • Creams V 2.0
    • Elixers V 2.0
    • Ointments V 2.0
    • Raw Material Warehouse V 2.0
    • Tablet Manufacturing V2.0

    New Publication: A must for All.

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