SOP for Reviewing Cleaning Validation Data – V 2.0

Procedure for Reviewing Cleaning Validation Data

Department	Quality Assurance (QA)/Validation/Quality Control (QC)/Production
SOP No.	SOP/Ointment/126
Supersedes	V 1.0
Page No.	Page X of Y
Issue Date	[Insert Issue Date]
Effective Date	[Insert Effective Date]
Review Date	[Insert Review Date]

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to define the process for reviewing cleaning validation data in ointment manufacturing. This ensures that cleaning procedures effectively remove residues, comply with regulatory standards, and maintain product safety.

2. Scope

This SOP applies to all personnel in the Quality Assurance (QA), Validation, Quality Control (QC), and Production departments responsible for reviewing, analyzing, and maintaining cleaning validation data.

3. Responsibilities

QA Officer: Reviews cleaning validation data for compliance with regulatory requirements.
Validation Team: Collects and compiles cleaning validation data.
QC Analyst: Conducts analytical testing and reports findings.
Production Supervisor: Ensures adherence to validated cleaning procedures.
QA Manager: Approves final validation reports and ensures documentation accuracy.

4. Accountability

The QA and Validation Managers are accountable for ensuring that cleaning validation data is reviewed as per GMP, FDA, ICH, and WHO guidelines.

5. Procedure

5.1 Collection of Cleaning Validation Data

Obtain validation data from multiple sources, including:
- Swab sampling results
- Rinse water analysis
- Total Organic Carbon (TOC) testing
- High-Performance Liquid Chromatography (HPLC) reports
- Microbial testing results
Ensure all data is recorded in cleaning validation log sheets.
Confirm that test parameters match

predefined acceptance criteria.

5.2 Data Analysis and Interpretation

Compare residue levels with established limits.
Identify any trends or deviations in data.
Assess consistency of validation results across multiple cleaning cycles.

5.3 Handling Deviations and Non-Conformances

Investigate any data points exceeding acceptance criteria.
Identify root causes of deviations (e.g., improper cleaning, equipment failure).
Initiate corrective and preventive actions (CAPA) if necessary.
Document all deviations and actions taken in the validation report.

5.4 Review and Approval of Cleaning Validation Data

QA must review all collected data for completeness and accuracy.
Validation and QC teams must verify analytical test results.
QA Manager must approve the final validation report before submission.

5.5 Documentation and Record Maintenance

Maintain validation reports in a controlled document repository.
Ensure data is readily available for regulatory audits and inspections.
Retain validation data as per regulatory retention requirements.

6. Abbreviations

GMP – Good Manufacturing Practices
QA – Quality Assurance
QC – Quality Control
TOC – Total Organic Carbon
HPLC – High-Performance Liquid Chromatography

7. Documents

Cleaning Validation Data Log (Annexure-1)
Cleaning Validation Summary Report (Annexure-2)

8. References

ICH Q7 – Good Manufacturing Practice Guide
WHO Guidelines for Cleaning Validation
US FDA Guidance on Cleaning Validation

9. SOP Version

Version 2.0

10. Approval Section

	Prepared By	Checked By	Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Cleaning Validation Data Log

Date	Equipment ID	Test Parameter	Result	Reviewed By
01/02/2025	MIX-1001	TOC Analysis	Pass	QA Manager
02/02/2025	FILL-2002	HPLC	Pass	QA Manager

Annexure-2: Cleaning Validation Summary Report

Equipment ID	Validation Test	Acceptance Criteria	Final Status	Approved By
MIX-1001	TOC Analysis	< 5 ppm	Pass	QA Manager
FILL-2002	HPLC	< 10 ppm	Pass	QA Manager

12. Revision History:

Revision Date	Revision No.	Details of Revision	Reason for Revision	Approved By
01/01/2024	1.0	Initial Version	New SOP	QA Head
01/02/2025	2.0	Updated SOP Format	Standardization of Document	QA Head