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SOP for Handling and Disposal of Waste in Lotions Production

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SOP for Handling and Disposal of Waste in Lotions Production

Standard Operating Procedure for Handling and Disposal of Waste in Lotions Production

1) Purpose

The purpose of this SOP is to establish guidelines for the proper handling, segregation, and disposal of waste generated during lotions production to ensure environmental protection and regulatory compliance.

2) Scope

This SOP applies to all personnel involved in the handling, segregation, and disposal of waste generated from lotions production activities within the pharmaceutical manufacturing facility.

3) Responsibilities

The responsibilities for executing this SOP are as follows:

Production Operators:

  • Segregate waste materials according to the categories specified in this SOP.
  • Dispose of waste materials in designated containers or areas as per regulatory requirements.
See also  SOP for Viscosity Testing of Lotions

Environmental Health and Safety (EHS) Personnel:

  • Provide training to personnel on waste handling and disposal procedures outlined in this SOP.
  • Monitor compliance with waste management practices and regulations.

Facility Management:

  • Ensure proper labeling, storage, and disposal of waste materials in accordance with local regulations and facility policies.

4) Procedure

4.1 Waste Segregation:

  • Segregate waste materials into categories such as general waste, hazardous waste, recyclable materials, and biohazardous waste.
  • Use designated bins or containers labeled with the appropriate waste category.

4.2 Disposal Guidelines:

  • Dispose of general waste in designated waste bins for landfill disposal.
  • Dispose of hazardous waste, including chemicals and solvents, in accordance with hazardous
waste management procedures.
  • Recycle materials such as cardboard, plastics, and glass as per facility recycling programs.
  • Handle biohazardous waste, such as contaminated materials, in compliance with biohazard waste disposal protocols.
  • 4.3 Waste Minimization:

    • Minimize waste generation by optimizing production processes and using materials efficiently.
    • Implement practices for reducing packaging waste and reusing materials where feasible.

    4.4 Spill Response:

    • Follow spill response procedures in case of accidental spills or leaks of hazardous materials.
    • Contain spills immediately and clean up using appropriate absorbent materials and personal protective equipment (PPE).

    4.5 Documentation:

    • Maintain accurate records of waste disposal activities, including waste manifests and disposal certificates.
    • Document incidents, spills, and corrective actions taken during waste handling and disposal.

    5) Abbreviations, if any

    SOP: Standard Operating Procedure

    EHS: Environmental Health and Safety

    PPE: Personal Protective Equipment

    6) Documents, if any

    • Waste Disposal Records
    • Waste Manifests
    • Incident Reports

    7) Reference, if any

    • Environmental Protection Agency (EPA) regulations on hazardous waste management
    • Local waste disposal regulations and guidelines

    8) SOP Version

    Version 1.0

    See also  SOP for Conducting Process Validation for Lotions
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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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