Validation Report

TEM060 Issue date

Validation Report

(Ref.VAL005)

Project Name		Project Number
Equipment		Serial Number
Manufacturer		Model Number
Process Line/Location		Protocol number

Table of Content

PROCESS DESCRIPTION ........................................................................................................................................2 OBJECTIVE...........................................................................................................................................................2 INSTRUMENTATION/CALIBRATION ..........................................................................................................................2 TEST FUNCTIONS PERFORMED IN THE OPERATIONAL QUALIFICATION PHASE AND OVERALL RESULTS OBTAINED .......2 ADDITIONAL VALIDATION REQUIREMENTS ..............................................................................................................2 OVERALL CONCLUSION .........................................................................................................................................3 REVALIDATION PROGRAM .....................................................................................................................................3

Approval of The Completed Operational Qualification Report
Department	Name	Signature	Date
Project Coordinator
Validation Manager
Quality Assurance Manager
Operations Manager
Production Manager

Approval signifies provisional approval of the equipment / system for production use.

File Location: Date Printed: Page 1 of 3

TEM060 Issue date

Validation Report

(Ref.VAL005)

Established	fulfilled and approved by the Production Manager
Training conducted	Yes / No – Sign & Date
All SOP’s established	Yes / No – Sign & Date

Overall Conclusion

Acceptance criteria for the overall program shall be based on the following:

1. Successful precalibration data for all critical test instrumentation
2. Successful completion of all test functions listed in Part 4.
3. Successful postcalibration of all critical test instrumentation.

Tabulate and review all data referenced above. Form a conclusion as to the acceptability of the overall program based on the acceptance criteria specified above.

Conclusion:

(Text)

Revalidation Program

Revalidation of this equipment / system is required:

• when the findings of inprocess and quality control tests indicate the need or
• routinely

Tests Required	Frequency

Completed Validation Report:

	Position	Signature	Date
Documented by
Checked by

File Location: Date Printed: Page 3 of 3