Document Management Procedure Template – Free Sample Download

how to get a document management procedure template

In this article, you will learn how to download and use Document Management Procedure Template to improve the Quality Systems of FDA-regulated companiesMoreover, you can learn how to get a free Document Management Software Application to handle your GMP documentation records and activities fast and easily.

WHAT IS A DOCUMENT MANAGEMENT PROCEDURE TEMPLATE?

The cGMP Document Management procedure template is a downloadable document ready to use and customize to handle your company’s needs of employees training as per 21 CFR Part 211 Sub Part J – Records and Reports and Part 820.40  — Subpart D – Document Controls.

This document is fully editable in MS Word and contains copyright information only authorized to use within your company site.  Another distribution outside your company is prohibited.

TEMPLATE DOCUMENT PURPOSE

This procedure provides instructions for the creation and implementation of document control activities. The implementation activities include the delivery, maintenance, evaluation, and storage of document content.  To download a free cGMP Document procedure template sample in .pdf format, click here.  

In addition, with it, you can verify that the processes involved in the company activities are properly documented in all applicable forms and fields to be filled.

This procedure brings the requirements for the identification, execution, and evaluation of the effectiveness of documentation activities.

Moreover, it shall provide the mechanism to document the document history records of each procedure and approved signature in a signature log.

Template Document Scope  

This procedure applies to all employees that perform any GxP function or responsibilities. These functions include any activity required to accomplish the tasks and duties assigned to the corresponding quality and operations departments.

It also applies to any other departments that provide or performs any GxP Documentation Control activities (e.g. human resources, production, engineering, quality department, etc).

Here is the table of contents of the cGMP Document management procedure template.

CIQA Document and Records Control Management Procedure Template - index page_Page_02
CIQA Document and Records Control Management Procedure Template – index page_Page_02

To download a free cGMP Document Management Procedure Template sample in .pdf format, click here.  

HOW TO AVOID MISTAKES IMPLEMENTING A DOCUMENT MANAGEMENT  PROCEDURE.

  1. We suggest evaluating your current process, activities and responsibilities to determine which quality management procedures, forms, and work instructions, are in each area, but, also consider the frequency of review them.
  2. If you have a small number of records and document, you can initiate a GMP documentation management manually using hard paper.  In case you need to create or update your cGMP Document Management Procedure, you can use a template procedure to accelerate the process to implement a manual Document Management System.

ORDER ONLINE DOCUMENT MANAGEMENT PROCEDURES & TEMPLATES

Now you can download a Document Management Procedures Templates fully editable in MS Word or get a hard-copy and Amazon Kindle format, ready to fill, and use according to your cGMP needs, check the following documents and see more information at the CIQA Shop. 


Training Management Procedure SOP Template front page


Order a Hard copy document


Download in MS Word or .pdf


Order Amazon Kindle Version


CIQA All You Need to Know About Training Management System


Order a Hard copy document


Order Amazon Kindle Version

DOCUMENT MANAGEMENT SOFTWARE APPLICATION

Moreover, you can get a free Document Management Software Application to handle all your document records from anywhere at any time.  Subscribe to learn more about our free document management software application.



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CIQA is a quality and regulatory consultant with 25 years of experience developing products and managing projects in the medical device supply chain, and pharmaceutical industries. Rest assured of the safety or being in the right hands.

IF YOU HAVE ANY QUESTIONS ABOUT DOCUMENT MANAGEMENT, FEEL FREE TO CONTACT US EITHER BY EMAIL OR PHONE: 787-487-9235.  (Hablamos Español)

REFERENCES

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Ramon Cayuela, MS, BS, Chemical Engineering

Ramon Cayuela, MS, BS, Chemical Engineering

CIQA President and CEO.
I've been working in validation engineering since 1992 with many multinational pharmaceutical companies. I love sharing my passion and knowledge with others. If you have any questions about anything (or just have general questions). I will be more than happy to assist you. You can count on the BEST customer service on CIQA. I go to great lengths to make sure my clients are 100% satisfied with their purchases and check emails/messages consistently throughout the day. You can rest assured that everything being sold here is as-described or your money back. I look forward to working with you!

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