GxP Responsibilities Procedure Template NFT – MSWord

This GxP Responsibilities Procedure Template is the first NFT downloadable MSWord document ready to use and handle all your needs to establish the responsibilities related to Good Manufacturing Practices, Good Documentation Practices, Good Laboratory Practices, etc.  Now you can implement rapidly a formal GxP Responsibilities Program with pre-established instructions and guidelines as per ISO 13485 Standards, 21 CFR part 211, 820, and FDA regulations in pharmaceutical and medical devices companies.

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Get a collectible full-version document as NFT, available in the following formats: Adobe.pdf or Microsoft Word.

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Once you pay online for this NFT digital asset in the NFT marketplace, you can download the SOP Procedure Template file on your computer for a fast implementation of it on your company site.

A GREAT INVESTMENT. Since it is a limited collectible edition, you can resell it in the NFT marketplace and generate profits in the future.

This utility NFT document contains copyright information only authorized to use within your company site.  Another distribution outside your company is prohibited, other than reselling the same NFT in the marketplace.

Download a free sample of validation protocol procedures templates


The GxP Responsibilities Procedure Template is an NFT (Non-Fungible Token) downloadable MSWord document ready to use and manage your Good (Manufacturing, laboratory, documentation, etc)  Practices activities in a planned and systematic manner.  This 15-page document is the first collectible digital asset of a GxP Responsibilities Management Procedure Template (Limited Edition) available in MS Word and Adobe .pdf format from the NFT marketplace.   It contains copyright information only authorized to use within your company site.

To download a free sample of the GxP Responsibilities Procedure Template, click here.  

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This procedure template is an NFT digital asset intended to set forth the instructions to manage and implement the GxP Responsibilities. It describes step-by-step the methodology for periodically and randomly examining QSR Quality System Regulations’ practices, records, and operations to determine the responsibility’s effectiveness.

Purpose of the GxP Responsibilities Procedure Template

The purpose of this document is to provide instructions and a guide to designate the responsibilities for each record and activity contained in the GxP document approved. Besides, this procedure must guarantee:

• The duties are valid, reasonable, written, and approved under the consent and agreement of the company management and involved parties.

• The responsibilities are clear, specific, accurate, and described appropriately and annotated in English.

• The responsibilities designation is properly addressed, documented, and satisfactorily established after considering all affected applications and documents.

GxP Responsibilities Procedure Template Scope and Topics

The scope of this document aims to all GxP documents generated by the corporate during the system development life cycle, including, but not limited to: software design specification documents, manuals, procedures, testing, and validation-related documents.

The responsibilities designation also aims to ensure the project completion on the expected due date and to accomplish the commitment on each task and activity under consideration by the correct responsible person(s).

The responsibilities designation is divided into two (2) primary groups:

• The responsibilities of the document originator that is designated to prepare, execute and close a particular GxP document.

• The responsibilities of the document reviewer or approver that is designated to double-check everything, including but not limited to: guaranteeing that the document complies with all requirements established in the company procedures.

Additional responsibilities groups or roles can be defined and used as needed by each particular GxP document.

Important Note:

Once you implement your GxP Responsibilities Program using this procedure template, you can resell the same NFT if you want in the NFT marketplace to make profits from your investment.

In addition, it allows you the mechanism to handle the GxP Responsibilities and activities been identified that need to be considered and mitigated.

Don’t lose this extraordinary investment opportunity to get a utility NFT procedure template written by the experienced author: Ramon Cayuela, CIQA Director.

Buy now.

Download a free sample of validation protocol procedures templates

Avoid Mistakes Implementing a GxP Responsibilities Management Program.

Review your Quality GxP Responsibilities Procedures. Evaluate all your current and previous activities, but also the QSR Quality System Regulation’s requirements that need to be considered and documented.

Moreover, evaluate the frequency of your documentation, risks, and how fast you need to perform and close each record, with its pending items.

Visit www.ciqa.net/shop to download other Quality Management Procedure Templates in .pdf format or fully editable in MS Word format, ready to fill, and use according to your cGMP needs at affordable prices.


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QMS Software Applications

The GxP Responsibilities documentation and its records management can be handled either manually or electronically using QMS software applications.  For more information about  Quality Management System (QMS) Software Applications, click here.

Quality Management System QMS Software Application
Quality Management System QMS Software Application

About The Author:

Ramon Cayuela Melendez, CIQA Director

Ramon Cayuela Melendez, CIQA Director

Bachelor’s and Master’s Degrees in Chemical Engineering from the University of Mayaguez, Puerto Rico.

30+ years of experience in Quality System Regulations serving more than 1,000 clients in over 100 multinational companies related to pharmaceutical, biotechnology, food & medical devices.

Manager & Senior Scientist with proficient skills and experience in Pharmaceutical Validations, Quality Assurance, Regulatory Compliance, Research & Development (R&D), GMP/ISO Audits, CAPA, Automation & Software Development.

Author of over 250 Quality Management Procedures and Validation Protocols Templates NFTs.

United States & European Citizens.  Speak English & Spanish.



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CIQA is a validation, quality, and regulatory compliance company with over 30 years of experience bringing consulting services to the pharmaceutical, medical device, and biotechnology industries.



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Adobe .pdf, Microsoft Word