Quality Management System Procedure Issue Date: Rev.

[Laboratory Name] YYYY/MM/DD x

Title: Page #:
Type in the title of Your Document 1 of x

Prepared by: Date:

Reviewed by: Date:

Approved by: Date:

The colored ink stamp indicates this is a controlled document. Absence of color indicates this copy
is not controlled and will not receive revision updates.

Purpose
Document the purpose of the procedure.

Scope / Field of Application

Document the scope/field of application.

Definitions and Acronyms

Document the appropriate definitions or acronyms associated with this procedure.
SOP: standard operating procedure

Responsibilities
Document any responsibilities.

Materials Required
Document the materials required to perform this procedure.
SOPs following this format will match the quality management system set out in the ISO 17025
Quality Manual Template. Go to www.e-shoq.com to obtain the ISO 17025 Quality Manual
Template.

Effective Date: YYYY/MM/DD

 Quality Management System Procedure Issue Date: Rev.:

[Laboratory Name] YYYY/MM/DD x

Title: Page #:
Type in the title of Your Document 2 of x

Procedure
Document the procedure.

Documentation
The following Quality Records shall be generated and managed:

Required Record Custodian

Quality Manual www.e-shoq.com

Other
Additional headings can be created by the user of this template.

Headings that are not applicable can be deleted.

Reference Procedures
List any procedures that are necessary or useful in conjunction with this procedure.

References
This standard operating procedure template has been provided by SHOQ Quality Assurance
Manuals Inc. The ISO 17025 Quality Manual Template that provides the framework to the quality
management system can be obtained at:

www.e-shoq.com

Revision History
Revision 0

Effective Date: YYYY/MM/DD