The process, which is carried out if necessary, is performed by the method of analyzing the specified conditions of use and assessing the conformity of product characteristics to these requirements, the result is the conclusion about the possibility of using the product for specific conditions. But which co nditions ?
Pharmaceutical Q.A - SOP perpn for Manufacturing & Quality Control . AHU validation as per GMP / GLP schedule .
Jaydip Datta thank you for your answer but validation uses just in pharmaceutical practice ?
Dr.Hikmat Abdulkarim Almadhkhori
I am sorry i dont understand you. 0)
The definition of this word in itself affirms legitimacy, authenticity and legalization.
For example validating the account.
Account validation in social networks includes checking that you are a real person, not a robot. In this case, in the window that appears, you must enter your mobile phone number. A free SMS will be sent with the confirmation code that you will need to write on the same website. At the same time
We always resort to checking the materials that we acquire, especially those related to materials that are eaten or come into contact with the human body, or at least we verify the dates of their validity.
As well as making sure that the characteristics of the product conform to the requirements.
Greetings
I,agree with Osamah K.Abdulretha Alshoreefi .
"I agree with Osama K. Abdul Ritha Al Sharif," Answer well.
Greetings
verification and validation are independent procedures that are used together for checking that a product, service, or system meets requirements and specifications and that it fulfills its intended purpose.[1] These are critical components of a quality management system such as ISO 9000. The words "verification" and "validation" are sometimes preceded with "independent", indicating that the verification and validation is to be performed by a disinterested third party. "Independent verification and validation" can be abbreviated as "IV&V".
In practice, as quality management terms, the definitions of verification and validation can be inconsistent. Sometimes they are even used interchangeably
Validation is actual confirmation of our claims using some standard procedures.
Process validation is defined as the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products. learnaboutgmp.com › good-validation-practices › the-four-types-of-pro...
The Four Types of Process Validation - Learnaboutgmp: Accredited ...
Process validation is the analysis of data gathered throughout the design and manufacturing of a product in order to confirm that the process can reliably output products of a determined standard. Regulatory authorities like EMA and FDA have published guidelines relating to process validation.[1] The purpose of process validation is to ensure varied inputs lead to consistent and high quality outputs. Process validation is an ongoing process that must be frequently adapted as manufacturing feedback is gathered. End-to-end validation of production processes is essential in determining product quality because quality cannot always be determined by finished-product inspection. Process validation can be broken down into 3 steps: process design, process qualification, and continued process verification.
Validation is concise "All in one" word which is commonly used in various fields of science and arts for defining limitation of certain things.
For example in pharmaceutical view point it can be used as for expiry date.
In Physics & Chemistry, it may be used as applicability.
In Data Science it can be used as model/method/function/algorithm performance up to some satisfactory level or no?...e.g., Model validation on some domain values is a particular test (e.g., classification, clustering, detection or tracking etc.,) weather the model is fit and performing well with good accuracy or no?
Process validation is the analysis of data gathered throughout the design and manufacturing of a product in order to confirm that the process can reliably output products of a determined standard. ...
Process validation is an ongoing process that must be frequently adapted as manufacturing feedback is gathered.
It is the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.
The term validation is used in various fields. In manufacturing it is the testing of product to see if it performs as advertised under different conditions. The reliability of the product as well as the repeatability in performance are at stake. In analytical work one tests the validity of a method by testing the model or method against experimental or observed data to validate the model or method.
I think that validating the test method is the process by which the relevance and reliability of the method are evaluated for a specific purpose. It is an essential stage in the evolution of the method from its development to its acceptance and application for organizational purposes.
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