Skip to content
  • Clinical Studies
  • Schedule M
  • Stability Studies
  • Pharma GMP
  • Pharma Tips
  • Pharma Books
  • Pharma Validation
  • Pharma Regulatory

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Handling Highly Potent Substances

Posted on By

SOP for Handling Highly Potent Substances

SOP for Handling Highly Potent Substances

1) Purpose

To establish procedures for the safe handling, storage, and disposal of highly potent substances to ensure employee safety and regulatory compliance.

2) Scope

This SOP applies to all personnel involved in the handling of highly potent substances within the pharmaceutical manufacturing facility.

3) Responsibilities

Environmental Health and Safety (EHS) Department: Responsible for developing and implementing safety protocols and conducting regular risk assessments.
Manufacturing Personnel: Responsible for adhering to procedures outlined in this SOP and participating in training programs.
Quality Assurance: Responsible for auditing and ensuring compliance with SOP requirements.
Facility Management: Responsible for ensuring adequate infrastructure and equipment for safe handling of potent substances.

See also  SOP for Tablet Coating Machine

4) Procedure

  1. Risk Assessment and Control Measures:

    1. Conduct a risk assessment to identify hazards associated with each potent substance.
    2. Implement engineering controls such as containment systems, ventilated enclosures, and closed systems.
    3. Provide appropriate personal protective equipment (PPE) including gloves, goggles, and respiratory protection.
  2. Handling Procedures:

    1. Receive and store potent substances in designated areas with restricted access.
    2. Label all containers clearly with substance name, potency, hazard
warnings, and expiration date.
  • Use dedicated equipment and tools for handling potent substances.
  • Minimize exposure through proper handling techniques and containment.
  • Spill and Emergency Response:

    1. Develop spill response procedures and ensure availability of spill kits.
    2. Train personnel on spill response protocols and evacuation procedures.
    3. Report all spills and incidents immediately to EHS and follow cleanup procedures.
  • Disposal and Waste Management:

    1. Segregate waste according to hazard classification and disposal requirements.
    2. Dispose of potent substances and contaminated materials in compliance with regulatory guidelines.
    3. Document disposal activities and maintain records of waste manifests.
  • 5) Abbreviations, if any

    SOP – Standard Operating Procedure

    EHS – Environmental Health and Safety

    PPE – Personal Protective Equipment

    6) Documents, if any

    • Risk Assessment Report
    • Training Records
    • Spill Response Plan
    • Waste Disposal Manifests

    7) Reference, if any

    OSHA Standard 29 CFR 1910.1200 – Hazard Communication

    8) SOP Version

    Version 1.0

    See also  SOP for Suppository Cooling Rack
    Vaginal Dosage Forms Tags:Audit trail SOP for vaginal dosage forms, Batch record review SOP for vaginal formulations, Batch release procedure for vaginal gels, Change control SOP for vaginal products, Cleaning validation SOP for vaginal equipment, Complaint handling SOP for vaginal products, Deviation handling SOP for vaginal dosage forms, Documentation control SOP for vaginal SOPs, environmental monitoring in vaginal manufacturing, Filling suppositories, GMP SOP for vaginal gel manufacturing, Labeling SOP for vaginal medicines, Mixing SOP for vaginal formulations, Packaging SOP for vaginal dosage forms, Procedure for vaginal ring production, Process validation SOP for vaginal preparations, Quality control SOP for vaginal tablets, Risk assessment SOP for vaginal manufacturing, SOP for emergency response in vaginal production, SOP for filling vaginal suppositories, SOP for vaginal cream formulation, SOP for vaginal dosage forms, SOP for vaginal medications, SOP for vaginal production, Stability testing SOP for vaginal rings, Sterility testing SOP for vaginal products, Suppository SOP, Training program for vaginal product manufacturing, Vaginal suppository manufacturing SOP, Vaginal tablet production guidelines, Validation protocol for vaginal creams, Vendor qualification SOP for vaginal ingredients

    Post navigation

    Previous Post: SOP for Equipment Qualification Protocols
    Next Post: SOP for Tertiary Packaging Machine

    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

    Read SOPs in your Language:

     - 
    Bengali
     - 
    bn
    English
     - 
    en
    Gujarati
     - 
    gu
    Hindi
     - 
    hi
    Malayalam
     - 
    ml
    Marathi
     - 
    mr
    Punjabi
     - 
    pa
    Tamil
     - 
    ta
    Telugu
     - 
    te

    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.

    Copyright © 2025 SOP Guide for Pharma.

    Powered by PressBook WordPress theme

    Go to mobile version