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SOP for Inventory Control in MDI Production

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SOP for Inventory Control in MDI Production

Inventory Management Procedures for MDI Production

1) Purpose

The purpose of this SOP is to establish procedures for inventory control in metered-dose inhaler (MDI) production to ensure accurate tracking, storage, and management of materials and finished products.

2) Scope

This SOP applies to all inventory management activities within the MDI production facility, including raw materials, intermediates, packaging materials, and finished products.

3) Responsibilities

The responsibilities for this SOP include maintaining inventory accuracy, conducting regular counts, ensuring proper storage conditions, and documenting all inventory transactions.

4) Procedure
4.1 Inventory Tracking

4.1.1 Implement an inventory management system to track the receipt, storage, and usage of materials and finished products.

See also  SOP for Personnel Hygiene in MDI Production

4.1.2 Assign unique identification numbers or barcodes to all inventory items for accurate tracking and traceability.

4.2 Receiving Materials

4.2.1 Verify the quantity and quality of incoming materials against purchase orders and specifications upon receipt.

4.2.2 Record all received materials in the inventory management system and update stock levels accordingly.

4.3 Storage Conditions

4.3.1 Store materials and finished products under appropriate conditions to maintain their quality and integrity, following specified storage requirements such as temperature, humidity, and light exposure.

4.3.2 Segregate materials based on their status (e.g., quarantined, approved, rejected) and compatibility to prevent cross-contamination.

4.4 Inventory Issuance and Usage

See also  SOP for Process Optimization for MDIs

4.4.1 Implement procedures for

issuing materials to production areas, ensuring accurate recording of quantities and batch numbers.

4.4.2 Monitor inventory usage regularly to detect discrepancies and take corrective actions if necessary.

4.5 Inventory Counts

4.5.1 Conduct regular physical inventory counts (e.g., monthly, quarterly) to verify actual stock levels against recorded levels in the inventory management system.

4.5.2 Investigate and resolve any discrepancies identified during inventory counts, documenting the findings and corrective actions taken.

4.6 Disposal of Obsolete or Expired Inventory

4.6.1 Identify and segregate obsolete, expired, or damaged materials and products for proper disposal according to regulatory requirements and company policies.

4.6.2 Update the inventory management system to reflect the disposal and adjust stock levels accordingly.

See also  SOP for Labeling of MDIs

4.7 Documentation and Records

4.7.1 Maintain accurate records of all inventory transactions, including receipts, issuances, returns, and disposals.

4.7.2 Document any deviations from SOPs related to inventory control and implement corrective actions as necessary.

5) Abbreviations, if any

MDI: Metered-Dose Inhaler

SOP: Standard Operating Procedure

6) Documents, if any

Inventory management system records, receiving logs, inventory count sheets, disposal records, and corrective action reports should be maintained as part of the inventory control process.

7) Reference, if any

Refer to inventory management guidelines from regulatory agencies, industry standards (e.g., GMP), 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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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

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