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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Environment, Health and Safety

SOP for Maintaining Maintenance Records for Safety Equipment

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The purpose of this SOP is to establish a standardized procedure for maintaining accurate and up-to-date maintenance records for safety equipment to ensure operational reliability, compliance with regulatory standards, and workplace safety.
Click to read the full article.

Environment, Health and Safety

SOP for Preparing Compliance Certificates for EHS Programs

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The purpose of this SOP is to establish a standardized procedure for preparing compliance certificates for Environmental, Health, and Safety (EHS) programs to ensure adherence to regulatory standards and demonstrate organizational commitment to EHS practices.
Click to read the full article.

Environment, Health and Safety

SOP for Filing Corrective Action Reports Post-Incident

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The purpose of this SOP is to establish a structured process for documenting and filing corrective action reports (CARs) after an incident to ensure root cause analysis, implementation of corrective actions, and prevention of recurrence.
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Environment, Health and Safety

SOP for Preparing and Submitting Environmental Impact Reports

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The purpose of this SOP is to establish a systematic approach for preparing and submitting Environmental Impact Reports (EIRs) to evaluate potential environmental consequences of organizational activities and ensure compliance with regulatory standards.
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Environment, Health and Safety

SOP for Preparing EHS Budget and Financial Records

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The purpose of this SOP is to establish a standardized process for preparing and managing Environmental, Health, and Safety (EHS) budgets and financial records, ensuring efficient allocation of resources, transparency, and compliance with financial policies.
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Environment, Health and Safety

SOP for Updating Documentation Based on Regulatory Changes

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The purpose of this SOP is to establish a systematic approach for reviewing, updating, and maintaining documentation to align with regulatory changes, ensuring compliance and organizational consistency.
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Environment, Health and Safety

SOP for Archiving Expired or Obsolete Safety Documents

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The purpose of this SOP is to establish a standardized process for archiving expired or obsolete safety documents to ensure proper record management, compliance with regulatory standards, and ease of retrieval when needed.
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Environment, Health and Safety

SOP for Preparing and Maintaining Audit Trail for EHS Activities

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The purpose of this SOP is to establish a systematic process for creating and maintaining an audit trail for Environmental, Health, and Safety (EHS) activities to ensure accountability, transparency, and compliance with regulatory and organizational standards.
Click to read the full article.

Environment, Health and Safety

SOP for Preparing Reports on Energy and Resource Conservation

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The purpose of this SOP is to outline a systematic approach for preparing detailed reports on energy and resource conservation initiatives, enabling organizations to evaluate their efforts, demonstrate compliance, and identify areas for improvement.
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Environment, Health and Safety

SOP for Documenting and Reporting Near-Miss Incidents

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The purpose of this SOP is to establish a standardized procedure for documenting and reporting near-miss incidents to identify potential hazards, prevent future accidents, and promote a culture of safety within the organization.
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Environment, Health and Safety

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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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