Standard Operating Procedure for Color Consistency Testing in Transdermal Patches

1) Purpose

The purpose of this SOP is to establish procedures for evaluating the color consistency of transdermal patches to ensure uniform appearance and quality.

2) Scope

This SOP applies to color consistency testing conducted during the manufacturing and quality control of transdermal patches within the facility.

3) Responsibilities

The Quality Control (QC) Department is responsible for executing color consistency testing as per this SOP. Production personnel provide samples and facilitate testing activities.

4) Procedure

4.1 Sample Selection

• 4.1.1 Obtain representative samples of transdermal patches from production batches according to approved sampling procedures.
• 4.1.2 Ensure samples represent different lots, if applicable, to cover variations in formulation or production conditions.

4.2 Visual Assessment

• 4.2.1 Evaluate each sample visually under standardized lighting conditions to assess color appearance and uniformity.
• 4.2.2 Compare sample colors against a master reference sample or color standards established for transdermal patches.

4.3 Instrumental Analysis (if applicable)

• 4.3.1 Use color measurement instruments, such as spectrophotometers or colorimeters, for quantitative assessment of color attributes.
• 4.3.2 Ensure instruments are calibrated and validated according to established procedures before conducting measurements.

4.4 Acceptance Criteria

• 4.4.1 Determine acceptance criteria for color consistency based on internal standards, customer requirements, or regulatory guidelines.
• 4.4.2 Reject batches not meeting