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SOP for Pest Control in MDI Production Area

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SOP for Pest Control in MDI Production Area

Pest Control Procedures in MDI Production Area

1) Purpose

The purpose of this SOP is to establish procedures for pest control in the metered-dose inhaler (MDI) production area to prevent contamination and ensure compliance with regulatory requirements.

2) Scope

This SOP applies to all areas within the MDI production facility, including production rooms, storage areas, and surrounding premises.

3) Responsibilities

The responsibilities for this SOP include implementing pest control measures, monitoring for pests, and maintaining records of pest control activities.

4) Procedure
4.1 Pest Inspection and Monitoring

See also  SOP for Storage Conditions of MDIs

4.1.1 Conduct regular inspections of production areas and adjacent spaces for signs of pests.

4.1.2 Use appropriate monitoring tools such as traps, baits, and pheromone traps to detect pest activity.

4.2 Pest Control Measures

4.2.1 Implement integrated pest management (IPM) strategies, including sanitation, exclusion, and chemical control methods.

4.2.2 Use approved pesticides and baits according to manufacturer instructions and regulatory guidelines.

4.3 Record Keeping

4.3.1 Maintain accurate records of pest control activities, including inspection reports, treatment dates, pest sightings, and corrective actions taken.

4.3.2 Document any deviations from pest control procedures and actions to address them.

4.4 Training and Awareness

See also  SOP for Formulation Development for MDIs

4.4.1 Provide training to personnel on pest control procedures, identification of pests, and reporting of pest sightings.

4.4.2 Promote awareness among staff about the

importance of pest control in maintaining product quality and safety.

5) Abbreviations, if any

MDI: Metered-Dose Inhaler

SOP: Standard Operating Procedure

IPM: Integrated Pest Management

6) Documents, if any

Pest control logs, inspection reports, pesticide application records, training records, and corrective action logs should be maintained as part of the quality management system.

7) Reference, if any

Refer to pest control guidelines from regulatory agencies, such as FDA, EPA, and local health authorities.

8) SOP Version

See also  SOP for Stability Testing of MDIs

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
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  • BA-BE Studies V 2.0
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