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SOP for Handling and Disposal of Waste in Transdermal Patches Production

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SOP for Handling and Disposal of Waste in Transdermal Patches Production

Standard Operating Procedure for Handling and Disposal of Waste in Transdermal Patches Production

1) Purpose

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

2) Scope

This SOP applies to all waste generated in the manufacturing process of transdermal patches, including raw material waste, packaging waste, and process waste.

3) Responsibilities

The Production Manager is responsible for overseeing the implementation of waste handling and disposal procedures. All personnel involved in waste management must adhere to this SOP.

See also  SOP for Quality Control Testing of Transdermal Patches

4) Procedure

4.1 Waste Segregation and Collection

  • 4.1.1 Segregate different types of waste (e.g., chemical, biological, general) at the point of generation using designated containers.
  • 4.1.2 Label each waste container with the type of waste, date, and area of origin.
  • 4.1.3 Use color-coded bins or labels to distinguish between different types of waste as per regulatory requirements.

4.2 Storage of Waste

  • 4.2.1 Store waste containers securely in designated storage areas that are inaccessible to unauthorized personnel.
  • 4.2.2 Ensure that storage areas are well-ventilated, fire-safe, and equipped with spill containment measures.
  • 4.2.3 Monitor and maintain waste storage areas to prevent leaks, spills, or environmental contamination.
See also  SOP for Process Optimization for Transdermal Patches

4.3

Waste Disposal

  • 4.3.1 Dispose of hazardous waste (e.g., solvents, chemicals) according to local regulatory requirements and guidelines.
  • 4.3.2 Contract with authorized waste disposal vendors for proper collection, transportation, and disposal of hazardous and non-hazardous waste.
  • 4.3.3 Complete waste disposal manifests and other required documentation for tracking and regulatory compliance.

4.4 Spill Response

  • 4.4.1 Develop and maintain a spill response procedure for accidental spills of hazardous materials.
  • 4.4.2 Train personnel on spill response protocols, including containment, cleanup, and reporting procedures.
  • 4.4.3 Document all spill incidents, including root cause analysis and corrective actions taken.

4.5 Training and Awareness

  • 4.5.1 Provide training to personnel involved in waste handling and disposal on the proper segregation, storage, and disposal practices.
  • 4.5.2 Conduct periodic refresher training sessions and maintain records of training attendance.
See also  SOP for Scale-Up Processes in Transdermal Patches Production

4.6 Compliance and Documentation

  • 4.6.1 Maintain records of waste generation, handling, and disposal activities, including waste manifests, disposal certificates, and training records.
  • 4.6.2 Conduct regular audits and inspections to ensure compliance with SOPs and regulatory requirements.
  • 4.6.3 Review and update the SOP as necessary based on changes in waste management practices or regulatory requirements.

5) Abbreviations, if any

SOP: Standard Operating Procedure

6) Documents, if any

Waste Manifests
Training Records

7) Reference, if any

EPA Guidelines for Hazardous Waste Management
WHO Guidelines on Health-Care Waste Management

8) SOP Version

Version 1.0

Transdermal Patches Tags:Adhesion Testing Protocol, Analytical Method Development SOP, Assay of Active Ingredient SOP, Contamination Prevention SOP, Documentation SOP, Equipment calibration SOP, Equipment Cleaning SOP, Final Product Inspection SOP, Formulation development SOP, Homogeneity Testing SOP, In-process Testing SOP, Microbial Testing SOP, Personnel Training SOP, Process Optimization SOP, Process Validation SOP, Quality Control Transdermal Patches, Raw Material Inspection SOP, Release Rate Testing SOP, Sample Collection SOP, Sterility Maintenance SOP, Storage Conditions Transdermal Patches, Thickness Testing Procedure, Transdermal Patch Manufacturing SOP, Transdermal Patch Stability Testing, Waste Handling SOP

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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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