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SOP for Inventory Control in Creams Production

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SOP for Inventory Control in Creams Production

Standard Operating Procedure for Inventory Control in Creams Production

1) Purpose

The purpose of this SOP is to establish guidelines and procedures for effective inventory control of raw materials, packaging materials, and finished products used in creams production to ensure accurate tracking, optimal stock levels, and compliance with regulatory requirements.

2) Scope

This SOP applies to all personnel involved in the management and control of inventory within the creams production facility.

3) Responsibilities

The Inventory Control Manager is responsible for overseeing inventory control processes, ensuring accuracy, and maintaining optimal stock levels. Warehouse staff are responsible for accurately recording inventory movements and conducting regular stock counts.

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4) Procedure

4.1 Inventory Recording

4.1.1 Record all inventory transactions (receipts, issues, returns, adjustments) in the inventory management system promptly and accurately.

4.1.2 Ensure that each inventory entry includes details such as material name, batch number, quantity, and transaction date.

4.2 Stock Levels Monitoring

4.2.1 Regularly review stock levels to ensure they are within the established minimum and maximum limits.

4.2.2 Generate inventory reports to monitor stock levels and identify trends or issues.

4.2.3 Reorder materials proactively to avoid stockouts and production delays.

4.3 Inventory Counting

4.3.1 Conduct regular physical inventory counts to verify the accuracy of inventory records.

4.3.2 Schedule and perform cycle counts for

high-value or high-turnover items.

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4.3.3 Document and investigate any discrepancies between physical counts and inventory records, and take corrective actions as necessary.

4.4 Inventory Reconciliation

4.4.1 Reconcile inventory records with physical counts at regular intervals (e.g., monthly, quarterly).

4.4.2 Adjust inventory records to reflect the actual stock levels based on reconciliation results.

4.4.3 Report significant discrepancies to management and implement measures to prevent recurrence.

4.5 Inventory Management Best Practices

4.5.1 Implement a First-In-First-Out (FIFO) or First-Expiry-First-Out (FEFO) system to manage inventory rotation.

4.5.2 Ensure that all inventory storage areas are organized, labeled, and clean.

4.5.3 Use barcoding or RFID technology to enhance inventory tracking and accuracy.

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4.6 Handling and Storage

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

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

4.6.3 Implement proper handling procedures to prevent damage to materials and ensure safety.

5) Abbreviations, if any

FIFO: First-In-First-Out

FEFO: First-Expiry-First-Out

RFID: Radio-Frequency Identification

6) Documents, if any

Inventory Records

Stock Level Reports

Cycle Count Reports

Reconciliation Reports

7) Reference, if any

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

ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients

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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