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SOP for Cleaning of Equipment Used for Gels

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SOP for Cleaning of Equipment Used for Gels

Standard Operating Procedure for Cleaning of Equipment Used for Gels

1) Purpose

The purpose of this SOP is to establish procedures for the cleaning of equipment used in the manufacturing of gels to prevent cross-contamination, ensure product quality, and comply with regulatory standards.

2) Scope

This SOP applies to all personnel involved in the cleaning of equipment used for gel production within the pharmaceutical manufacturing facility.

3) Responsibilities

Production Supervisor: Oversee equipment cleaning procedures as per this SOP.
Production Operators: Perform equipment cleaning and inspection tasks.
Quality Assurance (QA) Personnel: Verify cleaning effectiveness and compliance with procedures.

See also  SOP for Visual Inspection of Gels

4) Procedure

4.1 Pre-Cleaning Preparation
4.1.1 Wear appropriate personal protective equipment (PPE) such as gloves and safety goggles.
4.1.2 Notify production and quality personnel of equipment to be cleaned and its status.

4.2 Cleaning Process
4.2.1 Dismantle equipment parts as per the cleaning procedure and SOP.
4.2.2 Remove residual product and contaminants using approved cleaning agents and tools.
4.2.3 Rinse equipment thoroughly with purified water to remove cleaning agents and residues.

4.3 Disinfection
4.3.1 Apply disinfectants as specified in the cleaning SOP to sanitize equipment surfaces.
4.3.2 Ensure adequate contact time for disinfectants as per manufacturer’s recommendations.

4.4 Inspection and Assembly
4.4.1 Inspect cleaned equipment visually for cleanliness and signs of damage or wear.
4.4.2 Reassemble equipment components carefully and according to assembly instructions.

See also  SOP for Preventing Contamination in Gels Production

4.5 Verification and Documentation
4.5.1 Perform swab or rinse sampling to verify the effectiveness of cleaning and disinfection.
4.5.2 Document cleaning and disinfection activities, including any deviations or corrective actions.

4.6 Storage and Post-Cleaning Practices
4.6.1 Store cleaned equipment in designated areas to prevent re-contamination.
4.6.2 Follow post-cleaning procedures to maintain equipment integrity and readiness for use.

5) Abbreviations, if any

SOP: Standard Operating Procedure
PPE: Personal Protective Equipment
QA: Quality Assurance

6) Documents, if any

– Equipment Cleaning and Disinfection Records
– Swab/Sample Test Results
– SOP for Equipment Cleaning

7) Reference, if any

– FDA Guidance for Industry: Cleaning Validation
– USP <1072> Disinfectants and Antiseptics
– Manufacturer’s instructions for cleaning agents and disinfectants

See also  SOP for Documentation Control 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
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  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
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  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
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  • 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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