ISO 9001 Certification – Preventive Maintenance Register

An ISO 9001 preventive maintenance register is a document or a record used to keep track of preventive maintenance activities carried out on equipment, machines, or other assets in an organization. The register typically includes information such as:

1. Equipment identification - this includes details such as the asset name, serial number, or location.

2. Maintenance schedule - the date, frequency, and type of maintenance required to keep the equipment in good working condition.

3. Maintenance history - a record of all maintenance activities carried out, including the date, time, and details of the maintenance performed.

4. Maintenance personnel - the name of the person or team responsible for performing the maintenance.

5. Inspection results - the results of any inspections carried out on the equipment, including any issues or problems identified and the corrective action taken.

6. Documentation - any documents or manuals related to the equipment or maintenance activities, such as user manuals, maintenance instructions, or repair logs.

7. Calibration - any calibration activities carried out on the equipment, including the date and results of calibration tests.

A preventive maintenance register is an important tool for organizations to ensure that their equipment is maintained to the highest standards and to prevent equipment failure or downtime. It helps to ensure that equipment is regularly serviced and inspected, which can improve its performance, extend its lifespan, and reduce the risk of costly repairs or replacements.

How to get ISO 9001 Certification

Getting ISO 9001 certification is a long process; it may take a minimum of three to four months to complete the certification process. As an experienced ISO 9001 consultant , LMG can help you achieve the ISO 9001 certification process at a reasonable cost and a minimum timeframe.

ISO 9001 Certificate

The international organization for standardization (ISO) only develops the standards, and certification is not a requirement. Still, manufacturing and service companies require a document to present to their customers as evidence of ISO 9001 implementation. Third-party certification bodies issue the ISO 9001 certificate as evidence of ISO implementation after conducting an audit per ISO guidelines.

Our Services include.

• ISO 9001 Consulting
• ISO 13485 Certification
• ISO 20000 Certification
• ISO 22000 Certification
• ISO 27000 Certification

• GMP Certification
• US FDA Certification
• CE Certification
• 21 CFR 820 Consulting
• 21 CFR 211 Consulting

• 510 K Consulting
• FDA DMF Consulting
• FDA Drug Consulting
• FDA Cosmetics Certification
• FDA Medical Device Registration

For more information, Please contact us with detailed information.