CIP Skid (Sterile/LVP) – PQ Protocol

Document ID: PQ-CIP-001

Version: 1.0

Effective Date: [Insert Date]

Review Date: [Insert Date]

Prepared By: [Insert Name]

Approved By: [Insert Name]

Performance Qualification Protocol for CIP Skid in IV Infusions

Tags: Equipment Validation, Performance Qualification, CIP Skid, IV Infusions

Objective

The objective of this protocol is to validate the performance of the CIP Skid utilized for the automated cleaning of tanks and lines in the production of IV infusions, ensuring compliance with regulatory standards and operational efficiency.

Scope

This protocol applies to the CIP Skid used in the production area for cleaning processes related to LVP/SVP IV infusion bags and bottles.

Responsibilities

The Validation Team is responsible for executing this protocol, while the Quality Assurance Team will oversee compliance and documentation. Production personnel are responsible for the operation of the equipment during testing.

Prerequisites

  • Completion of Installation Qualification (IQ) for the CIP Skid.
  • Training of personnel on equipment operation and safety protocols.
  • Availability of cleaning agents and validation equipment.

Equipment Description

The CIP Skid is a sterile system designed for the automated cleaning of tanks and lines used in the production of IV infusions. It includes features for flow control, temperature regulation, conductivity measurement, and cycle time management.

Test Plan

Test ID Procedure Acceptance Criteria Evidence
TP-001 Verify flow rate during cleaning cycle. Flow rate within specified limits. Flow rate log.
TP-002 Check temperature during cleaning cycle. Temperature within specified limits. Temperature log.
TP-003 Measure conductivity before and after cleaning. Conductivity meets specifications. Conductivity log.
TP-004 Audit trail verification. Complete and accurate audit trail. Audit trail report.
TP-005 Cycle time verification. Cycle time within specified limits. Cycle time log.
See also  Laminator / Backing Attachment Unit – OQ Protocol

Detailed Test Cases

Test Case: Flow Rate Verification

Measure the flow rate during the cleaning cycle using calibrated flow meters. Record readings at specified intervals. Acceptance criteria: Flow rate must be within ±10% of the target value.

Test Case: Temperature Check

Monitor the temperature of the cleaning solution during the cycle using calibrated thermometers. Acceptance criteria: Temperature must remain within ±2°C of the target value.

Test Case: Conductivity Measurement

Measure the conductivity of the cleaning solution before and after the cleaning cycle. Acceptance criteria: Conductivity must meet predetermined specifications.

Test Case: Audit Trail Verification

Review the audit trail generated during the cleaning cycle to ensure all operations are recorded accurately. Acceptance criteria: No discrepancies in the audit trail.

Test Case: Cycle Time Verification

Document the total time taken for each cleaning cycle. Acceptance criteria: Cycle time must not exceed specified limits.

Deviations

Any deviations from the acceptance criteria must be documented, with an investigation to determine the cause and corrective actions to be implemented.

Approvals

Prepared By: [Insert Name] – Signature: ___________ Date: ___________

Approved By: [Insert Name] – Signature: ___________ Date: ___________

Data Integrity Checks

  • Ensure all data is recorded in validated systems.
  • Implement regular backups of audit trails and logs.
  • Conduct periodic reviews of data integrity protocols.