SOP Guide for Pharma

SOP for Equipment Logbook Maintenance

SOP for Equipment Logbook Maintenance

Standard Operating Procedure for Equipment Logbook Maintenance

1) Purpose

The purpose of this SOP is to establish procedures for the maintenance of equipment logbooks used in the manufacturing of dental dosage forms, ensuring accurate recording of equipment activities and compliance with regulatory standards.

2) Scope

This SOP applies to all equipment logbooks maintained for manufacturing equipment used in the production of dental pastes, gels, and mouthwashes within the pharmaceutical industry.

3) Responsibilities

The Production Department is responsible for maintaining equipment logbooks. The Quality Assurance (QA) Department is responsible for reviewing logbook entries periodically to ensure completeness and accuracy.

4) Procedure

4.1 Logbook Setup and Entries

4.1.1 Assign a dedicated logbook for each piece of manufacturing equipment.

4.1.2 Enter equipment identification details, including name, model, and location, in the logbook header.

4.2 Daily Operations Recording

4.2.1 Record daily operational activities, including start-up, shutdown, cleaning, maintenance, and calibration, in the logbook.

4.2.2 Document any deviations, incidents, or abnormalities encountered during equipment operations.

4.3 Calibration and Maintenance Records

4.3.1 Log calibration and maintenance activities performed on equipment, including dates, personnel involved, and results.

4.3.2 Attach calibration and maintenance certificates or reports to the logbook entries as applicable.

4.4 Equipment Changeover Records

4.4.1 Document equipment changeover procedures and associated activities in the logbook.

4.4.2 Record the start and end

times of changeover operations, including cleaning and setup activities.

4.5 Review and Approval

4.5.1 Review logbook entries regularly to ensure completeness, accuracy, and compliance with procedures.

4.5.2 Approve logbook entries and sign off to confirm review by authorized personnel.

5) Abbreviations, if any

SOP – Standard Operating Procedure

QA – Quality Assurance

6) Documents, if any

Equipment Logbooks

Calibration and Maintenance Reports

Changeover Procedures

7) Reference, if any

Current Good Manufacturing Practices (cGMP) guidelines

Company-specific equipment logbook policies

8) SOP Version

Version 1.0

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