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SOP for Analytical Method Development for Gels

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SOP for Analytical Method Development for Gels

Standard Operating Procedure for Analytical Method Development for Gels

1) Purpose

The purpose of this SOP is to outline procedures for the development and validation of analytical methods used for testing gels to ensure accurate and reliable analytical results.

2) Scope

This SOP applies to all personnel involved in analytical method development for gels within the pharmaceutical manufacturing facility.

3) Responsibilities

Analytical Chemist: Lead analytical method development and validation activities.
Quality Assurance (QA) Team: Review and approve analytical method validation protocols and reports.
Formulation Scientists: Provide input on method requirements based on formulation characteristics.

See also  SOP for Regulatory Laboratory Controls and Testing

4) Procedure

4.1 Method Development
4.1.1 Define analytical requirements based on product specifications and regulatory guidelines.
4.1.2 Evaluate and select appropriate analytical techniques (e.g., HPLC, GC, spectroscopy).

4.2 Method Optimization
4.2.1 Optimize analytical parameters such as mobile phase composition, wavelength, and column temperature.
4.2.2 Conduct feasibility studies to ensure methods are suitable for routine analysis.

4.3 Method Validation
4.3.1 Validate analytical methods according to ICH guidelines or relevant compendia.
4.3.2 Perform validation parameters including specificity, linearity, accuracy, precision, and robustness.

4.4 Documentation and Reporting
4.4.1 Document method development and validation activities in detail.
4.4.2 Prepare comprehensive validation reports summarizing method performance and validation outcomes.

See also  SOP for Residual Solvent Testing

5) Abbreviations, if any

SOP: Standard Operating Procedure
QA: Quality Assurance
HPLC: High-Performance Liquid Chromatography
GC: Gas Chromatography

6) Documents, if any

– Analytical Method Development Protocols
– Method Validation Reports
– Feasibility and Optimization Studies

7) Reference, if any

– ICH Q2(R1): Validation of Analytical Procedures
– USP General Chapter <1225> Validation of Compendial Procedures
– Company-specific analytical method development guidelines and procedures

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
  • 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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