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Quality Assurance: SOP for pH Testing of Gels

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SOP for pH Testing of Gels

Standard Operating Procedure for pH Testing of Gels

1) Purpose

The purpose of this SOP is to outline procedures for pH testing of gels in the pharmaceutical industry to ensure product quality and consistency.

2) Scope

This SOP applies to all personnel involved in pH testing of gels within the pharmaceutical production facility.

3) Responsibilities

Quality Control (QC) Supervisor: Oversee pH testing procedures as per this SOP.
QC Analysts: Perform pH tests and record results accurately.
Production Operators: Provide gel samples and support as required for pH testing.

4) Procedure

4.1 Equipment Setup
4.1.1 Verify and calibrate the pH meter according to manufacturer instructions.
4.1.2 Prepare fresh pH buffers of known pH values (e.g., pH 4, 7, and 10) for calibration.

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4.2 Sample Preparation
4.2.1 Allow gel samples to equilibrate to room temperature before testing.
4.2.2 Mix samples gently to ensure homogeneity without introducing air bubbles.

4.3 pH Measurement
4.3.1 Rinse the pH electrode with distilled water and blot dry between measurements.
4.3.2 Immerse the pH electrode into the gel sample and allow the reading to stabilize.
4.3.3 Record pH readings once stabilized and repeat measurements as necessary for accuracy.

4.4 Calibration

of pH Meter
4.4.1 Calibrate the pH meter using the prepared pH buffers before each testing session.
4.4.2 Verify calibration with fresh buffers and adjust if necessary to maintain accuracy.

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4.5 Data Analysis and Acceptance Criteria
4.5.1 Compare pH measurements against predefined acceptance criteria or specifications.
4.5.2 Identify and document any deviations from specified pH limits.

4.6 Cleaning and Maintenance
4.6.1 Clean the pH meter electrode with distilled water and store it properly after each use.
4.6.2 Perform regular maintenance and calibration of the pH meter as per schedule.

5) Abbreviations, if any

SOP: Standard Operating Procedure
QC: Quality Control

6) Documents, if any

– pH Test Reports
– Calibration Certificates
– Equipment Cleaning and Maintenance Logs
– SOP for pH Testing

7) Reference, if any

– USP <791> pH
– Pharmacopoeial guidelines for pH testing of pharmaceuticals
– Manufacturer’s instructions for pH meter operation and calibration

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8) SOP Version

Version 1.0

Quality Assurance 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
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  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
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  • Nanoparticle Formulation
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  • Pharmacovigilance
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  • 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

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