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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Laboratory safety guidelines

SOP for Incident Investigation and Reporting in Microbiology Lab

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Standard Operating Procedure for Incident Investigation and Reporting in Microbiology Lab Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures for investigating and reporting microbial contamination incidents in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in incident investigation and reporting, including microbiologists, quality assurance personnel, and…

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Microbiology Testing

SOP for Environmental Cleaning Validation

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Standard Operating Procedure for Environmental Cleaning Validation Purpose The purpose of this Standard Operating Procedure (SOP) is to provide a protocol for validating the effectiveness of environmental cleaning procedures in the microbiology laboratory of the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in environmental cleaning validation activities, including laboratory technicians, microbiologists,…

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Microbiology Testing

SOP for Microbiological Method Validation

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Standard Operating Procedure for Microbiological Method Validation Purpose The purpose of this Standard Operating Procedure (SOP) is to provide instructions for validating microbiological testing methods in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in the validation of microbiological testing methods, including microbiologists, laboratory technicians, and quality assurance personnel. Responsibilities Quality…

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Microbiology Testing

SOP for Microbial Monitoring of Personnel

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Standard Operating Procedure for Microbial Monitoring of Personnel Purpose The purpose of this Standard Operating Procedure (SOP) is to establish protocols for monitoring the microbial flora of personnel involved in manufacturing processes within the pharmaceutical facility. Scope This SOP applies to all personnel working in areas where microbial contamination poses a risk to product quality…

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Microbiology Testing

SOP for Microbial Strain Verification

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Standard Operating Procedure for Microbial Strain Verification Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for verifying the identity and purity of microbial strains used in testing within the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in the procurement, storage, handling, and testing of microbial strains…

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Microbiology Testing

SOP for Laboratory Safety

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Standard Operating Procedure for Laboratory Safety Purpose The purpose of this Standard Operating Procedure (SOP) is to establish procedures and guidelines for ensuring the safety of personnel working in the microbiology laboratory within the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel working in the microbiology laboratory, including microbiologists, laboratory technicians, and support…

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Microbiology Testing

SOP for Microscopic Examination

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Standard Operating Procedure for Microscopic Examination Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines and procedures for examining microbial cultures under a microscope in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in microscopic examination procedures within the pharmaceutical manufacturing facility. Responsibilities Quality Control (QC) Department:…

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Microbiology Testing

SOP for Culture Preservation

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Standard Operating Procedure for Culture Preservation Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines for the preservation of microbial cultures for long-term storage in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in the preservation of microbial cultures, including microbiologists, laboratory technicians, and quality assurance personnel….

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Microbiology Testing

Microbiology Testing: SOP for Documentation and Record-Keeping

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Standard Operating Procedure for Documentation and Record-Keeping Purpose The purpose of this Standard Operating Procedure (SOP) is to establish guidelines for documenting and maintaining records of microbiological testing activities in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in microbiological testing, including microbiologists, laboratory technicians, and quality assurance personnel. Responsibilities Quality…

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Microbiology Testing

SOP for Microbial Culturing

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Standard Operating Procedure for Microbial Culturing Purpose The purpose of this Standard Operating Procedure (SOP) is to provide guidelines and procedures for culturing microorganisms from samples in the pharmaceutical manufacturing facility. Scope This SOP applies to all personnel involved in microbial culturing procedures within the pharmaceutical manufacturing facility. Responsibilities Quality Control (QC) Department: Responsible for…

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Microbiology Testing

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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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