Tablet Checkweigher (Inline) – OQ Protocol

Document Control:

  • Document Number: OQ-001
  • Version: 1.0
  • Effective Date: 2023-10-01
  • Review Date: 2024-10-01
  • Approved By: [Name]

Operational Qualification Protocol for Inline Tablet Checkweigher

Objective: To validate the operational performance of the Inline Tablet Checkweigher used for weight verification in the production of solid dosage forms.

Scope: This protocol applies to the Inline Tablet Checkweigher located in the Production/Compression area for direct product impact with criticality classified as critical.

Responsibilities:

  • Validation Team: Execute and document the qualification activities.
  • Quality Assurance: Review and approve the protocol and results.
  • Operations: Provide access to the equipment and necessary resources.

Prerequisites:

  • Completion of Installation Qualification (IQ).
  • Availability of operational procedures for the equipment.
  • Training of personnel on equipment usage and data handling.

Equipment Description: The Inline Tablet Checkweigher is designed for real-time weight verification of tablets during the production process. It features an accuracy reject mechanism and maintains an audit trail for compliance and traceability.

Test ID Procedure Acceptance Criteria Evidence
OQ-01 Verify accuracy of weight measurements using calibrated weights. Weight measurements must be within ±5% of the target weight. Calibration certificates and measurement logs.
OQ-02 Audit trail review for reject mechanism. Audit trail must show all rejected weights and actions taken. Audit trail report.

Detailed Test Cases:

  • Test Case OQ-01: Use calibrated weights to check the accuracy of the tablet checkweigher. Record the weights and compare against the target.
  • Test Case OQ-02: Review the audit trail for the reject mechanism to ensure all actions are documented and compliant with URS Annex11.
See also  Tablet/Capsule Counter Filler – Deviation Impact Assessment

Deviations: Any deviations from the acceptance criteria must be documented, with a thorough investigation conducted to determine the root cause and corrective actions taken.

Data Integrity Checks:

  • Ensure that all weight measurements are automatically logged with timestamps.
  • Verify the integrity of the audit trail by checking for unauthorized access or modifications.
  • Conduct regular backups of all data to prevent loss.

Approvals:

  • Validation Team Lead: ______________________ Date: __________
  • Quality Assurance: ______________________ Date: __________
  • Operations Manager: ______________________ Date: __________