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SOP for Consistency Testing in Creams

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SOP for Consistency Testing in Creams

Standard Operating Procedure for Consistency Testing in Creams

1) Purpose

The purpose of this SOP is to outline the procedures for testing the consistency of creams to ensure product uniformity and quality.

2) Scope

This SOP applies to all personnel involved in the quality control testing of creams, including laboratory technicians, analytical chemists, and quality assurance (QA) personnel. It covers procedures for sample preparation, consistency testing, and documentation.

3) Responsibilities

It is the responsibility of laboratory technicians to prepare and analyze samples, analytical chemists to validate the consistency testing method, and QA personnel to review and approve the test results.

4) Procedure

4.1 Preparation for Consistency Testing

4.1.1 Review the batch record and sampling plan to determine the number of samples to be analyzed.

4.1.2 Ensure all testing equipment (e.g., viscometer, penetrometer) is calibrated and in proper working condition.

See also  SOP for pH Testing of Creams

4.1.3 Prepare all necessary reagents and materials according to the validated method.

4.1.4 Label all sample containers with necessary information, including sample ID, batch number, and date of preparation.

4.1.5 Wear appropriate personal protective equipment (PPE) such as gloves, lab coat, and safety glasses to avoid contamination.

4.2 Sample Preparation

4.2.1 Weigh an appropriate amount of cream sample into a clean container, as specified in the validated consistency testing method.

4.2.2 Condition the sample by equilibrating it at the specified temperature (e.g., 25°C) for a set period.

4.2.3 Homogenize the sample to ensure a uniform mixture before testing.

4.3 Consistency Testing Methods

4.3.1 Viscometer Method:

4.3.1.1 Set up the viscometer according to the manufacturer’s instructions and the validated method parameters.

4.3.1.2 Introduce the conditioned cream sample into the viscometer.

See also  SOP for Particle Size Distribution in Creams

4.3.1.3 Measure the viscosity of the cream at different shear rates or rotational speeds, as specified in the validated method.

4.3.1.4 Record the viscosity readings and calculate the average viscosity.

4.3.2 Penetrometer Method:

4.3.2.1 Set up the penetrometer according to the manufacturer’s instructions and the validated method parameters.

4.3.2.2 Place the conditioned cream sample in the penetrometer container.

4.3.2.3 Lower the penetrometer needle or cone onto the surface of the cream and measure the penetration depth after a specified time.

4.3.2.4 Record the penetration depth readings and calculate the average consistency.

4.4 Quality Control

4.4.1 Perform the consistency testing in duplicate or triplicate to ensure accuracy and precision.

4.4.2 Include quality control (QC) samples and reference standards in the analysis run to verify the reliability of the results.

4.4.3 Compare the consistency test results with the specification limits to determine if the batch meets the required criteria.

See also  SOP for Out of Specification (OOS) Handling in Creams Production

4.5 Documentation and Review

4.5.1 Document all details of the consistency testing procedure, including sample preparation, instrument settings, and measurement results, in the consistency testing log or laboratory notebook.

4.5.2 Review the consistency data and ensure all results are within the specified acceptance criteria.

4.5.3 Submit the consistency test results for review and approval by QA personnel.

4.5.4 Maintain records of the consistency test results according to company policy and regulatory requirements for future reference and audits.

5) Abbreviations, if any

QA: Quality Assurance

PPE: Personal Protective Equipment

SOP: Standard Operating Procedure

6) Documents, if any

Batch Records

Sampling Plan

Consistency Testing Log

Calibration Records

7) Reference, if any

ICH Q2(R1): Validation of Analytical Procedures: Text and Methodology

USP (United States Pharmacopeia) General Chapter on Consistency Testing

8) SOP Version

Version 1.0

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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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