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SOP for Warehouse Management for Creams Production

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SOP for Warehouse Management for Creams Production

Standard Operating Procedure for Warehouse Management in Creams Production

1) Purpose

The purpose of this SOP is to establish guidelines and procedures for the efficient and effective management of the warehouse used for storing raw materials, packaging materials, and finished creams products.

2) Scope

This SOP applies to all personnel involved in the storage, handling, and management of materials in the warehouse used for creams production.

3) Responsibilities

The Warehouse Manager is responsible for the overall management of the warehouse, ensuring proper storage conditions, inventory accuracy, and compliance with SOPs. Warehouse staff are responsible for the receipt, storage, and dispatch of materials as per defined procedures.

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4) Procedure

4.1 Receiving Materials

4.1.1 Inspect incoming materials for damage and verify against the purchase order and delivery note.

4.1.2 Record the receipt of materials in the inventory management system.

4.1.3 Quarantine materials pending quality control approval.

4.2 Storage of Materials

4.2.1 Store materials in designated areas based on their classification (e.g., raw materials, packaging materials, finished products).

4.2.2 Ensure that storage conditions (e.g., temperature, humidity) comply with the specifications for each material.

4.2.3 Implement a First-In-First-Out (FIFO) or First-Expiry-First-Out (FEFO) system for material rotation.

4.2.4 Clearly label all materials with identification details, including name, batch number, and expiry date.

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4.3 Inventory Management

4.3.1 Maintain

an accurate and up-to-date inventory management system.

4.3.2 Conduct regular inventory counts and reconcile any discrepancies.

4.3.3 Monitor stock levels and reorder materials as necessary to avoid shortages.

4.4 Dispatch of Materials

4.4.1 Prepare materials for dispatch according to production requirements.

4.4.2 Verify the accuracy of the dispatch list and ensure proper documentation accompanies the materials.

4.4.3 Record the dispatch of materials in the inventory management system.

4.5 Handling and Safety

4.5.1 Use appropriate handling equipment and techniques to prevent damage to materials.

4.5.2 Ensure that all warehouse staff are trained in material handling and safety procedures.

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4.5.3 Store hazardous materials separately and in compliance with regulatory requirements.

4.6 Cleaning and Maintenance

4.6.1 Maintain a clean and organized warehouse environment.

4.6.2 Implement a regular cleaning schedule and document cleaning activities.

4.6.3 Ensure all storage equipment and facilities are well-maintained and in good working condition.

5) Abbreviations, if any

FIFO: First-In-First-Out

FEFO: First-Expiry-First-Out

6) Documents, if any

Purchase Orders

Delivery Notes

Inventory Records

Dispatch Lists

Cleaning Logs

7) Reference, if any

US FDA CFR (Code of Federal Regulations) Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals

WHO Technical Report Series, No. 961, 2011: Annex 9 – Guidelines on Packaging for Pharmaceutical Products

8) SOP Version

Version 1.0

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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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