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SOP for Handling and Disposal of Waste in Aerosol Production

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SOP for Handling and Disposal of Waste in Aerosol Production

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

1) Purpose

The purpose of this SOP is to establish guidelines for the proper handling and disposal of waste generated during aerosol production in the pharmaceutical industry. This ensures compliance with environmental regulations and promotes a safe working environment.

2) Scope

This SOP applies to all personnel involved in aerosol production at [Company Name], including production operators, waste handlers, and environmental health and safety (EHS) personnel responsible for waste management.

3) Responsibilities

Production Supervisor: Oversees waste handling procedures and ensures compliance.
Waste Handlers: Responsible for segregating and disposing of waste according to SOP.
EHS Officer: Provides guidance on regulatory requirements and monitors waste management practices.

See also  SOP for Stability Testing of Aerosols

4) Procedure

4.1 Waste Segregation:
4.1.1 Segregate waste at the point of generation into appropriate categories (e.g., general, hazardous, recyclable).
4.1.2 Use designated containers and labeling for each waste type to prevent cross-contamination.

4.2 Storage:
4.2.1 Store waste temporarily in designated storage areas with proper labeling and containment.
4.2.2 Ensure storage areas are secure and accessible only to authorized personnel.

4.3 Handling and Transportation:
4.3.1 Use appropriate personal protective equipment (PPE) when handling hazardous waste.
4.3.2 Transport waste to designated disposal areas or facilities

in accordance with local regulations.

4.4 Disposal:
4.4.1 Dispose of general waste through approved municipal waste management services.
4.4.2 Arrange for disposal of hazardous waste through licensed hazardous waste disposal contractors.

See also  SOP for Determination of Particle Size Distribution for Aerosols

4.5 Documentation:
4.5.1 Maintain records of waste generation, segregation, and disposal activities.
4.5.2 Document disposal receipts and certificates from authorized disposal facilities.

5) Abbreviations, if any

SOP: Standard Operating Procedure
EHS: Environmental Health and Safety
PPE: Personal Protective Equipment

6) Documents, if any

Waste Management Log
Disposal Certificates
Batch Manufacturing Record (BMR)

7) Reference, if any

Local Environmental Regulations
Occupational Safety and Health Administration (OSHA) guidelines for waste management

8) SOP Version

Version 1.0

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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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