Validation of process: Difference between revisions
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'''Validation of [[process]]''' is the process of verifying that a business process meets predetermined standards and criteria. This verification is necessary to ensure that the process is optimized for achieving the desired results. | '''Validation of [[process]]''' is the process of verifying that a business process meets predetermined standards and criteria. This verification is necessary to ensure that the process is optimized for achieving the desired results. | ||
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Despite its challenges, process improvement is still an essential component of any successful business. By understanding its benefits and drawbacks, and by carefully planning and executing improvement strategies, organizations can unlock the potential of their processes and ensure their success in the long run. | Despite its challenges, process improvement is still an essential component of any successful business. By understanding its benefits and drawbacks, and by carefully planning and executing improvement strategies, organizations can unlock the potential of their processes and ensure their success in the long run. | ||
== | {{infobox5|list1={{i5link|a=[[Service quality control]]}} — {{i5link|a=[[Software maintenance management]]}} — {{i5link|a=[[Methodology for process improvement]]}} — {{i5link|a=[[Reliability of measurement]]}} — {{i5link|a=[[Software quality model]]}} — {{i5link|a=[[Design for quality]]}} — {{i5link|a=[[Continuous improvement of quality]]}} — {{i5link|a=[[Quality and compliance]]}} — {{i5link|a=[[Certification of management system]]}} }} | ||
==References== | |||
* Sadiq, S. W., Orlowska, M. E., & Sadiq, W. (2005). ''[https://www.researchgate.net/profile/Shazia-Sadiq/publication/222394746_Specification_and_validation_of_process_constraints_for_flexible_workflows/links/5d62474da6fdccc32ccf1d55/Specification-and-validation-of-process-constraints-for-flexible-workflows.pdf?_sg%5B0%5D=started_experiment_milestone&origin=journalDetail&_rtd=e30%3D Specification and validation of process constraints for flexible workflows]''. [[Information]] Systems, 30(5), 349-378. | * Sadiq, S. W., Orlowska, M. E., & Sadiq, W. (2005). ''[https://www.researchgate.net/profile/Shazia-Sadiq/publication/222394746_Specification_and_validation_of_process_constraints_for_flexible_workflows/links/5d62474da6fdccc32ccf1d55/Specification-and-validation-of-process-constraints-for-flexible-workflows.pdf?_sg%5B0%5D=started_experiment_milestone&origin=journalDetail&_rtd=e30%3D Specification and validation of process constraints for flexible workflows]''. [[Information]] Systems, 30(5), 349-378. | ||
* Jatto, E., & Okhamafe, A. O. (2002). ''[https://www.ajol.info/index.php/tjpr/article/download/14592/16163 An Overview of Pharmaceutical Validation and Process Controls in Drug Development]''. Tropical Journal of Pharmaceutical Research, 1(2), 115-122. | * Jatto, E., & Okhamafe, A. O. (2002). ''[https://www.ajol.info/index.php/tjpr/article/download/14592/16163 An Overview of Pharmaceutical Validation and Process Controls in Drug Development]''. Tropical Journal of Pharmaceutical Research, 1(2), 115-122. | ||
* Aleem, H., Zhao, Y., Lord, S., McCarthy, T., & Sharratt, P. (2003). ''[https://www.researchgate.net/profile/Kamal-Badr/publication/333614160_Comparative_Study_of_Phenolic_Content_Antioxidant_potentials_and_Cytotoxic_Activity_of_the_Crude_and_Green_Synthesized_Silver_Nanoparticles'_Extracts_of_Two_Phlomis_Species_Growing_in_Egypt/links/5cf6cfec299bf1fb1859736c/Comparative-Study-of-Phenolic-Content-Antioxidant-potentials-and-Cytotoxic-Activity-of-the-Crude-and-Green-Synthesized-Silver-Nanoparticles-Extracts-of-Two-Phlomis-Species-Growing-in-Egypt.pdf Pharmaceutical process validation: an overview]''. Proceedings of the Institution of Mechanical Engineers, Part E: Journal of Process Mechanical Engineering, 217(2), 141-151. | * Aleem, H., Zhao, Y., Lord, S., McCarthy, T., & Sharratt, P. (2003). ''[https://www.researchgate.net/profile/Kamal-Badr/publication/333614160_Comparative_Study_of_Phenolic_Content_Antioxidant_potentials_and_Cytotoxic_Activity_of_the_Crude_and_Green_Synthesized_Silver_Nanoparticles'_Extracts_of_Two_Phlomis_Species_Growing_in_Egypt/links/5cf6cfec299bf1fb1859736c/Comparative-Study-of-Phenolic-Content-Antioxidant-potentials-and-Cytotoxic-Activity-of-the-Crude-and-Green-Synthesized-Silver-Nanoparticles-Extracts-of-Two-Phlomis-Species-Growing-in-Egypt.pdf Pharmaceutical process validation: an overview]''. Proceedings of the Institution of Mechanical Engineers, Part E: Journal of Process Mechanical Engineering, 217(2), 141-151. | ||
[[Category:Basic_concepts]] | [[Category:Basic_concepts]] |
Latest revision as of 06:33, 18 November 2023
Validation of process is the process of verifying that a business process meets predetermined standards and criteria. This verification is necessary to ensure that the process is optimized for achieving the desired results.
What is Validation of Process?
Validation of Process is a process that involves assessing a process to ensure that it is operating as intended and meeting established standards. It is important to employ this process in order to reduce the risk of errors and ensure that the process is compliant with relevant regulations.
The purpose of Validation of Process is to provide assurance that the process meets the desired quality standards. The process of Validation of Process can involve activities such as determining the design and performance of a system, validating the system, and verifying that it is operating as expected. This process includes steps such as identifying and assessing process requirements, developing process performance criteria, establishing process parameters and thresholds, and conducting tests to verify that the process meets the performance criteria.
Validation of Process is a must for any business that wants to make sure their processes are reliable, efficient, and cost-effective. It is the perfect way to ensure that the process is compliant with relevant regulations and reduce the risk of errors.
Applying Validation of Process in the Real World
It’s important to validate processes and systems to ensure that they are working correctly and producing reliable and accurate results. In the manufacturing industry, validation of process can be used to ensure that production lines are running correctly and that the products produced meet the required standards. Similarly, in the software development industry, validation of process can be used to ensure that software meets the required standards and all features work as expected. In the healthcare industry, validation of process can be used to ensure that medical instruments and procedures are functioning correctly and that the results produced are accurate.
There are several benefits to validating processes and systems. It can help to reduce costs and improve efficiency, as well as ensuring that results produced are reliable and accurate. This can lead to improved customer satisfaction and better overall performance.
Measuring Validation of Process
When it comes to process validation, there are a few key metrics to consider. Accuracy, effectiveness, efficiency, and maintenance should all be evaluated. Customer feedback surveys, customer satisfaction scores, customer retention rates, and process cycle times are all metrics that can be used to measure the validation of a process.
Data should be collected and analyzed to determine the effectiveness of the process and identify areas for improvement. It's important to note that process validation should not be a one-time event. It should be an ongoing process, with frequent reviews and adjustments as needed. Automated tools and software can be very useful in tracking and measuring the validation of a process over time.
With careful monitoring and measurement of process validation, businesses can ensure that their processes are delivering the intended results. By taking the time to assess performance and make necessary adjustments, companies can ensure that their processes are running effectively and efficiently. Taking the time to measure and validate processes is an important part of running a successful business.
Step-by-Step Guide to Validation of Process
Validation of process involves establishing baseline process objectives, collecting data on the process and its output, analyzing the data to identify any potential process improvements, making changes and re-testing, validating the changes, and then documenting the process.
The first step in the validation process is to establish the criteria that need to be met by the process and define the desired level of performance. This will provide a benchmark for measuring the success of the process. Once the baseline objectives have been established, data should be collected on the process and its output. This data will be used to analyze and identify any potential process improvements.
Once any changes have been identified and implemented, they should be tested and validated to confirm that the process is producing the desired outcome. This is an important part of the validation process, as it ensures that the changes have been implemented correctly and that the process is now producing the desired outcome.
Finally, it’s important to document the process and any changes that have been made. This will ensure that the process can be replicated in the future and that any changes can be traced back to their origin.
Pros and Cons of Validation of Process
When it comes to running a successful business, process improvement is key. Process improvement is an important part of any organization’s success, as it ensures that processes are reliable, efficient, and effective. But what exactly is process improvement and why is it so important?
Process improvement is the practice of analyzing and improving existing processes or developing new processes to increase efficiency, effectiveness, and reliability. It can be used to identify any potential risks or hazards associated with a process, as well as to ensure that processes are documented to ensure repeatability and consistency. Process improvement can also help to reduce costs by eliminating waste and improving quality and safety.
Although process improvement has many benefits, it can also be costly and time consuming. It requires detailed planning and oversight, as well as significant training and knowledge. It can also be difficult to implement and maintain, and may require modifications or updates to meet changing needs.
Despite its challenges, process improvement is still an essential component of any successful business. By understanding its benefits and drawbacks, and by carefully planning and executing improvement strategies, organizations can unlock the potential of their processes and ensure their success in the long run.
Validation of process — recommended articles |
Service quality control — Software maintenance management — Methodology for process improvement — Reliability of measurement — Software quality model — Design for quality — Continuous improvement of quality — Quality and compliance — Certification of management system |
References
- Sadiq, S. W., Orlowska, M. E., & Sadiq, W. (2005). Specification and validation of process constraints for flexible workflows. Information Systems, 30(5), 349-378.
- Jatto, E., & Okhamafe, A. O. (2002). An Overview of Pharmaceutical Validation and Process Controls in Drug Development. Tropical Journal of Pharmaceutical Research, 1(2), 115-122.
- Aleem, H., Zhao, Y., Lord, S., McCarthy, T., & Sharratt, P. (2003). Pharmaceutical process validation: an overview. Proceedings of the Institution of Mechanical Engineers, Part E: Journal of Process Mechanical Engineering, 217(2), 141-151.