Description

This BCP Performance Evaluation Procedure is an NFT (Non-Fungible Token) downloadable (Business Continuity Planning) MSWord document ready to use in an easy and systematic manner in pharmaceutical and medical device companies.   This 17-page document is the first collectible digital asset of the Performance Evaluation Procedure (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 BCP Performance Evaluation Procedure, click here.  

This procedure template is an NFT digital asset intended to set forth the instructions to manage and implement an effective Performance Appraisal Program.

It describes step-by-step the methodology for the implementation of a comprehensive Performance Evaluation strategy.

Purpose of the Performance Evaluation Procedure Template

The purpose of this BCP document is to evaluate the performance of each corrective action, mitigation activity, and preventive action implemented as part of the impact risk assessment, gap assessment, and business continuity plan.

The scope of this document is facilitating and prioritizing the systems and processes evaluation based on the FIPS 199 impact level and developing levels of recovery and strategies for minimizing loss. It provides guidelines on determining information and information system impact on organizational operations and assets, individuals, other organizations, and the nation through a formula that examines three security objectives: confidentiality, integrity, and availability.

Confidentiality preserves authorized restrictions on information access and disclosure, including means for protecting personal privacy and proprietary information.

Integrity guards against improper information modification or destruction, and includes ensuring information non-repudiation and authenticity.

Availability ensures timely and reliable access to and use of information.

Important Note:

This procedure template allows you to create a Performance Appraisal Program to identify and handle all information necessary to maintain your business up and running. Especially, it considers the manufacturing areas that need to be evaluated and documented as per cGMP recommendations.  Once you implement your Performance Appraisal Program using this procedure template, you can resell the same NFT if you want in the NFT marketplace to make profits of your investment.

 

 

SPECIAL BONUS

This procedure describes how to perform the activities related to Performance Appraisal Management in a practical way using template forms, as applicable to each case on your site.

 

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.

 

Avoid Mistakes Implementing a BCP Performance Appraisal Program.

Step 1. Review your actual Performance Evaluation Procedures and compare them against the applicable ISO 22301 Security and Resilience — Business Continuity Management Systems — Requirements.  Evaluate all your current and previous activities, but also the QSR Quality System Regulation’s requirements that need to be considered and documented frequently as per cGMP and FDA requirements.

Step 2. Evaluate the frequency of your Performance Evaluation activities to support your current strategy, documentation, risks, and how fast you need to perform and close each Performance Evaluation record, with its pending items.

Step 3. Implement a robust Performance Evaluation program with the correct monitoring, metrics, and corrective actions applicable to your site.

For more information, 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 BCP performance evaluation records can be handled either manually or electronically using QMS software applications.  For more information about  Quality Management System (QMS) Software Applications, click here.

 

About The Author:

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.

 

 

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.