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SOP for Pest Control Management

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SOP for Pest Control Management

Standard Operating Procedure for Pest Control Management

1) Purpose

The purpose of this SOP is to establish procedures for pest control management to prevent contamination and ensure a hygienic manufacturing environment.

2) Scope

This SOP applies to all personnel involved in pest control management at [Company Name] in the production of intramuscular, subcutaneous, and intravenous injection products.

3) Responsibilities

The responsibilities of this SOP include:
– Pest Control Team: Implementing and monitoring pest control measures.
– Quality Assurance (QA) Department: Reviewing and approving pest control procedures and records.
– Facility Maintenance: Ensuring structural integrity and hygiene of the manufacturing environment.

See also  SOP for Filtration of Solutions

4) Procedure

4.1 Pest Control Plan
4.1.1 Develop a pest control plan that includes preventive measures, monitoring, and control methods.
4.1.2 Identify areas susceptible to pest infestation and establish monitoring points.
4.2 Implementation of Pest Control Measures
4.2.1 Perform regular inspections of the facility to detect signs of pest activity.
4.2.2 Implement preventive measures such as sealing entry points, maintaining cleanliness, and eliminating food and water sources.
4.2.3 Use approved pest control products and methods to manage and eliminate pests.
4.3 Monitoring and Recording
4.3.1 Monitor pest control measures and document findings in pest control logs.
4.3.2 Record the type of pest, location, control

measures taken, and results of each inspection.
4.4 Evaluation and Continuous Improvement
4.4.1 Regularly review pest control logs and evaluate the effectiveness of pest control measures.
4.4.2 Update the pest control plan based on the evaluation and any new findings or infestations.
4.4.3 Conduct training for personnel on pest awareness and preventive measures.

See also  Injectables: SOP for Process Analytical Technology (PAT) Implementation

5) Abbreviations, if any

– QA: Quality Assurance

6) Documents, if any

– Pest Control Plan
– Pest Control Logs
– Inspection Reports

7) Reference, if any

– Good Manufacturing Practices (GMP) Guidelines
– International Organization for Standardization (ISO) Standards

8) SOP Version

Version 1.0

Injectables Tags:Analytical method validation for injections, Aseptic media fill trials SOP, Bioburden testing for injections, Cleaning validation for injection equipment, Emulsion stability testing for injections, Formulation development for injections, Homogeneity testing for injections, IM injection SOP, Injection filling volume accuracy, Injection stability testing, Intramuscular injection procedure, Intravenous injection guidelines, IV injection SOP, Needle assembly for syringes SOP, Packaging integrity testing for injections, Particle size analysis for injections, Pre-filled syringe stability testing, Product sterility in aseptic processing, Reconstitution testing for injections, SC injection SOP, Subcutaneous injection technique, Syringe filling and capping SOP, Syringe labeling and inspection SOP, Temperature mapping in storage areas, Viscosity testing for injections

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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
  • 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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