Standard Operating Procedure for Out of Specification (OOS) Handling in Transdermal Patches Production
1) Purpose
The purpose of this SOP is to establish a standardized procedure for the identification, investigation, and resolution of out-of-specification (OOS) results in the production and quality control of transdermal patches, ensuring compliance with regulatory requirements and maintaining product quality.
2) Scope
This SOP applies to all personnel involved in the production, quality control, and quality assurance of transdermal patches, as well as any other departments that may encounter OOS results during their activities.
3) Responsibilities
The Quality Assurance (QA) Department is responsible for overseeing the OOS handling process. All personnel are responsible for identifying, reporting, and investigating OOS results and cooperating in the resolution process.
4) Procedure
4.1 Identification and Reporting of OOS Results
- 4.1.1 Identify any test results that fall outside the established specifications or acceptance criteria during production or quality control testing.
- 4.1.2 Immediately report the OOS result to the supervisor and the QA Department using the OOS Report Form.
- 4.1.3 Document the details of the OOS result, including date, time, test method, and any immediate corrective actions taken, in the OOS Report Form.
4.2 Initial Laboratory Investigation
- 4.2.1 The QC Department conducts an initial laboratory
4.3 Full-Scale OOS Investigation
- 4.3.1 If the initial laboratory investigation does not identify an analytical error, initiate a full-scale OOS investigation involving a cross-functional team, including representatives from QA, Production, and QC.
- 4.3.2 Conduct a comprehensive review of the batch records, raw material quality, production process, and environmental conditions to identify potential causes of the OOS result.
- 4.3.3 Collect additional samples, if necessary, to perform retesting or further analysis. Document all investigation activities and findings in the OOS Investigation Report.
4.4 Root Cause Analysis and CAPA
- 4.4.1 Perform a root cause analysis to identify the underlying cause(s) of the OOS result, considering all potential factors from raw materials to finished product testing.
- 4.4.2 Develop and implement corrective actions to address the immediate cause of the OOS result and prevent recurrence.
- 4.4.3 Identify and implement preventive actions to eliminate the root cause and prevent similar OOS results in the future. Document all CAPA activities in the OOS Investigation Report.
4.5 Review and Approval
- 4.5.1 The QA Department reviews the completed OOS Investigation Report, including CAPA activities, to ensure adequacy and completeness.
- 4.5.2 Obtain final approval from the QA Manager or designee before closing the OOS report and releasing the batch for further processing or distribution.
4.6 Documentation and Trending
- 4.6.1 Maintain all OOS reports and related documentation in a centralized OOS Log.
- 4.6.2 Conduct periodic reviews and trend analysis of OOS results to identify patterns or areas for process improvement.
- 4.6.3 Implement process improvements based on trending analysis to enhance product quality and compliance.
5) Abbreviations, if any
SOP: Standard Operating Procedure
QA: Quality Assurance
QC: Quality Control
OOS: Out of Specification
CAPA: Corrective and Preventive Actions
6) Documents, if any
OOS Report Form
OOS Investigation Report
OOS Log
Batch Records
CAPA Documentation
7) Reference, if any
ICH Q10: Pharmaceutical Quality System
21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
FDA Guidance for Industry: Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
8) SOP Version
Version 1.0