Sop Template Version 01 Final

Quality Management
Documents & Templates
Title
Subtitle
Dear customer,
Thank you for purchasing this SOP template from QMdocs.
To assure a proper implementation of this SOP within your company’s Quality System please
follow the below described steps:
1. Save a copy of this template according to your file naming standards.
2. Exchange the existing QMdocs logo in the right header section with the logo of your
company.
3. Exchange left header section with your company name and department.
4. If you have legally purchased this SOP delete the copyright information in the footer
section, or replace it with your company’s copyright information.
5. Perform a careful review of the SOP and related content to assure you understand all
requirements.
6. Check whether all requirements are in compliance with your company’s general
standards and whether there are any conflicts to existing policies, standards or SOPs.
7. Complete the chapter 3 REGULATORY BASIS, REFERENCE DOCUMENTS with

internal references where applicable.
8. Exchange or fill green colored text with your company’s data.
9. Indicate the name and the department of the persons who will receive a controlled copy
of the finalized and approved SOP.
10. Assure SOP training before implementation.
11. Conduct an internal audit within an appropriate time after approval of the SOP to verify
whether the SOP requirements have been followed and if the deliverables are effective
and in compliance to your company’s expectations.
12. Delete this instruction note (first page).
Document Type Document ID Version Status Page

SOP XX_WWW_ZZZ_YYYY 1.0 Approved 1/6
Copyright © by QMdocs 2010

Reproduction, photocopying, storage or transmission by magnetic or electronic means strictly prohibited by law. Neither the document
nor the information contained therein may be reproduced or disclosed without written consent of QMdocs.
Quality Management
Title
Subtitle
AUTHORED BY: TITLE: DATE: SIGNATURE:
REVIEWED BY: TITLE: DATE: SIGNATURE:
Signs to confirm the content and

structure of this document
Signs to confirm the content and

structure of this document
APPROVED BY: TITLE: DATE: SIGNATURE:
Signs to confirm that this document is in

compliance with the Quality
Management System
DOCUMENT HISTORY
Effective Date Date Revision Required Supersedes
DD/MM/YYYY DD/MM/YYYY DD/MM/YYYY
Version Approval Date Description of the Change Author / Changed by
1.0 DD/MM/YYYY All Initial Document Name


Quality Management
Title
Subtitle
TABLE OF CONTENT
1 Purpose .....................................................................................................................................................4
2 Objective.....................................................................................................................................................4
3 Regulatory basis, reference documents ....................................................................................................4
4 Responsibility and accountability................................................................................................................4
5 Related documents.....................................................................................................................................5
6 Definitions...................................................................................................................................................5
7 Procedure...................................................................................................................................................5
7.1 Description of the Procedures and Processes.....................................................................6
8 Attachments................................................................................................................................................6
# 1 Title of attachment 1..........................................................................................................6
# 2 Title of attachment 2..........................................................................................................6
9 SOP distribution..........................................................................................................................................6
10 Health, safety and environmental considerations.....................................................................................6


Quality Management
Title
Subtitle
1 PURPOSE
This section describes the purpose of the Standard Operating Procedure.
2 OBJECTIVE
This paragraph should contain a description about the scope or objective of this Standard
Operating Procedure.
3 REGULATORY BASIS, REFERENCE DOCUMENTS

This section should include the regulatory references that were used to produce this SOP.
E.g.:
21 CFR 211.xx
21 CFR 211.113: Control of Microbiological Contamination
21 CFR 820.70 (c): Production and Process Controls, Environmental Control
EU GMP Guide § xyz
International Standard, ISO 14644-1, First edition, 1999-05-01
Clean room and Associated Controlled Environments, Part 1: Classification of Air Cleanliness,
2005 USP 28, U.S. Pharmacopoeia, <1116> Microbiological Evaluation of Clean Rooms and
Other Controlled Environments
4 RESPONSIBILITY AND ACCOUNTABILITY

This section should list all relevant participating parties within a company, their duties and
responsibilities related to this SOP and the described procedures and processes.
Quality Assurance (QA):
Review environmental monitoring data reports.
Ensure environmental monitoring investigations are appropriate and adequate, root causes are
identified and corrective actions are implemented.
Assess and close environmental monitoring investigations.


Quality Management
Title
Subtitle
5 RELATED DOCUMENTS
Table 1 : References to documents needed to proceed according to this procedure
Document ID Document Title
6 DEFINITIONS
Table 2: Glossary of Terminology used in the SOP
Term Description
21 CFR 210 &211
EU GMP Guide
ISO 13485
SOP
7 PROCEDURE


Quality Management
Title
Subtitle
7.1 Description of the Procedures and Processes

This Paragraph has a detailed description of the individual steps of the related process and
the instructions on how to execute the process.
8 ATTACHMENTS
#1 Title of attachment 1
#2 Title of attachment 2
9 SOP DISTRIBUTION
In this paragraph the customer should indicate the persons and department with authorized
copies of this SOP
SOP Authorized Copy Number Department Name
01 Production Mr. Sample
02
03
04
10 HEALTH, SAFETY AND ENVIRONMENTAL CONSIDERATIONS

This Paragraph should give relevant instructions in regard to related health, safety and
environmental conditions.



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Quality Management

Documents & Templates

1. Save a copy of this template according to your file naming standards.

7. Complete the chapter 3 REGULATORY BASIS, REFERENCE DOCUMENTS with

8. Exchange or fill green colored text with your company’s data.

10. Assure SOP training before implementation.

12. Delete this instruction note (first page).

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

AUTHORED BY: TITLE: DATE: SIGNATURE:

REVIEWED BY: TITLE: DATE: SIGNATURE:

Signs to confirm the content and

Signs to confirm the content and

APPROVED BY: TITLE: DATE: SIGNATURE:

Signs to confirm that this document is in

Effective Date Date Revision Required Supersedes

DD/MM/YYYY DD/MM/YYYY DD/MM/YYYY

Version Approval Date Description of the Change Author / Changed by

1.0 DD/MM/YYYY All Initial Document Name

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

3 REGULATORY BASIS, REFERENCE DOCUMENTS

4 RESPONSIBILITY AND ACCOUNTABILITY

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

Document ID Document Title

21 CFR 210 &211

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

7.1 Description of the Procedures and Processes

SOP Authorized Copy Number Department Name

01 Production Mr. Sample

10 HEALTH, SAFETY AND ENVIRONMENTAL CONSIDERATIONS

Document Type Document ID Version Status Page

Copyright © by QMdocs 2010

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