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SOP for Warehouse Management for MDI Production

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SOP for Warehouse Management for MDI Production

Warehouse Management Procedures for MDI Production

1) Purpose

The purpose of this SOP is to establish procedures for warehouse management in metered-dose inhaler (MDI) production to ensure efficient storage, handling, and control of raw materials, components, and finished products.

2) Scope

This SOP applies to all warehouse areas within the MDI production facility, including raw materials, packaging materials, intermediate products, and finished goods storage.

3) Responsibilities

The responsibilities for this SOP include inventory control, storage practices, material handling, and compliance with regulatory requirements.

4) Procedure
4.1 Warehouse Layout and Design

See also  SOP for Inventory Control in MDI Production

4.1.1 Designate specific storage areas for raw materials, components, intermediate products, and finished goods.

4.1.2 Ensure adequate space, shelving, and segregation based on material compatibility and storage requirements.

4.2 Receipt and Inspection of Materials

4.2.1 Receive incoming materials and verify against purchase orders, including quantity, specifications, and documentation requirements.

4.2.2 Conduct visual inspection and quality checks to ensure materials meet acceptance criteria before storage.

4.3 Storage Conditions

4.3.1 Store materials according to specified conditions (e.g., temperature, humidity, light exposure) as per product requirements and regulatory guidelines.

4.3.2 Monitor storage conditions regularly and implement controls to prevent mix-ups, cross-contamination, or deterioration.

4.4 Inventory Management

See also  SOP for Conducting Process Validation for MDIs

4.4.1 Maintain accurate inventory records, including receipts, withdrawals, and stock levels using a designated inventory management system.

4.4.2 Conduct

periodic physical inventory counts and reconciliation with electronic records to ensure accuracy.

4.5 Material Handling and Distribution

4.5.1 Implement procedures for safe handling, labeling, and transportation of materials within the warehouse.

4.5.2 Ensure proper documentation and traceability of materials during distribution to production areas or shipment to customers.

4.6 Environmental Controls

4.6.1 Monitor and control environmental factors such as temperature, humidity, and cleanliness to prevent adverse effects on stored materials.

4.6.2 Implement pest control measures and maintain cleanliness to minimize risks of contamination.

See also  SOP for Personnel Hygiene in MDI Production

4.7 Documentation and Records

4.7.1 Maintain detailed records of warehouse operations, including receipts, inspections, storage conditions, inventory transactions, and distribution activities.

4.7.2 Document any deviations from warehouse procedures and corrective actions taken to address them.

5) Abbreviations, if any

MDI: Metered-Dose Inhaler

SOP: Standard Operating Procedure

6) Documents, if any

Warehouse layout plans, inventory records, inspection reports, environmental monitoring logs, and material handling procedures should be maintained as part of the warehouse management system.

7) Reference, if any

Refer to warehouse management guidelines from regulatory agencies, industry standards (e.g., GDP), and internal quality management procedures.

8) SOP Version

Version 1.0

Metered-Dose Inhaler Tags:Analytical Method Development MDIs, Batch Manufacturing Record MDI, Calibration MDI Equipment, Cleaning Equipment MDIs, Color Consistency Testing MDI, Contamination Prevention MDI, Documentation MDI Manufacturing, Final Product Inspection MDI, Formulation Development MDI, In-process Testing Inhalers, Inhaler Manufacturing Procedures, Inhaler Quality Control SOP, Labeling MDI SOP, MDI Production SOPs, MDI Storage Conditions, Metered-Dose Inhaler SOP, Microbial Testing Inhalers, Packaging of MDIs Procedure, Particle Size Analysis MDIs, Preservative Efficacy MDIs, Process Optimization MDIs, Process Validation MDIs, Propellant Testing MDIs, Quality Testing MDIs, Raw Material Inspection MDIs, Solvents Use in MDI Production, Stability Testing MDIs, Sterility Maintenance MDI, Training Personnel MDI Production, Waste Disposal MDI Production

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Next Post: SOP for Facility Design and Layout

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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