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SOP for Handling and Disposal of Waste in Gels Production

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SOP for Handling and Disposal of Waste in Gels Production

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

1) Purpose

The purpose of this SOP is to establish procedures for the safe handling, segregation, and disposal of waste generated during the production of gels to minimize environmental impact and ensure compliance with regulatory requirements.

2) Scope

This SOP applies to all personnel involved in waste management within the pharmaceutical manufacturing facility where gels are produced.

3) Responsibilities

Environmental Health and Safety (EHS) Manager: Oversee waste management procedures and compliance with environmental regulations.
Production Operators: Segregate and handle waste according to this SOP.
Facility Maintenance Staff: Assist in waste disposal activities and ensure proper functioning of waste management systems.

See also  SOP for Sterility Testing in Aseptic Gels

4) Procedure

4.1 Waste Segregation
4.1.1 Segregate waste at the point of generation into categories (e.g., general, hazardous, recyclable).
4.1.2 Use color-coded bins or containers for easy identification and segregation.

4.2 Waste Collection
4.2.1 Collect segregated waste in designated containers or bins labeled with waste type and hazard classification.
4.2.2 Ensure containers are properly sealed and stored in designated storage areas.

4.3 Handling Procedures
4.3.1 Handle hazardous waste with appropriate PPE and according to safety data sheet (SDS) instructions.

/> 4.3.2 Minimize spills and emissions during waste handling and transfer operations.

4.4 Disposal Methods
4.4.1 Dispose of non-hazardous waste through approved waste management vendors or recycling programs.
4.4.2 Arrange for the safe disposal of hazardous waste through licensed waste disposal contractors.

See also  SOP for Energy Control Procedures in Gels Production

4.5 Emergency Response
4.5.1 Establish procedures for responding to spills, leaks, or accidents involving waste materials.
4.5.2 Train personnel on emergency response protocols and evacuation procedures if necessary.

4.6 Documentation and Records
4.6.1 Maintain records of waste generation, segregation, collection, and disposal activities.
4.6.2 Document incidents, spills, and corrective actions related to waste management.

5) Abbreviations, if any

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

6) Documents, if any

– Waste Management Logbook
– Hazardous Waste Manifests
– Training Records for Waste Handling

7) Reference, if any

– EPA Regulations on Hazardous Waste Management
– OSHA Guidelines for Hazardous Waste Operations and Emergency Response (HAZWOPER)
– Local regulations on waste disposal and environmental protection

See also  SOP for Scale-Up Processes in Gels Production

8) SOP Version

Version 1.0

Gels Tags:Analytical Method Development for Gels, Assay of Active Ingredient in Gels, Cleaning Equipment for Gel Production, Contamination Prevention in Gel Manufacturing, Equipment Calibration for Gel Manufacturing, Final Product Inspection for Gels, Gel Formulation Development, Gel Homogeneity Testing, Gel Labeling Procedures, Gel Preparation SOP, Gel Production Documentation, Gel Production Waste Disposal, Gel Quality Control Testing, Gel Viscosity Testing, In-process Testing for Gels, Microbial Testing of Gels, Packaging of Gels, Particle Size Analysis in Gels, Particle Size Distribution in Gels, pH Testing of Gels, Pharmaceutical Gel Manufacturing, Process Optimization for Gel Manufacturing, Process Validation for Gels, Raw Material Inspection for Gels, Rheological Testing in Gels, Sample Collection for Gel Quality Testing, Stability Testing for Gels, Sterility in Gel Production, Storage Conditions for Gels, Training for Gel Production Personnel

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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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