Open AccessA Review on Pharmaceutical Validation
Author(s) -
Sudarshan Balasaheb Kakad,
Mahesh Hari Kolhe,
Tushar Pradip Dukre
Publication year - 2020
Publication title -
international journal of pharmaceutical quality assurance
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.114
H-Index - 7
ISSN - 0975-9506
DOI - 10.25258/ijpqa.11.3.6
Subject(s) - process validation , pharmaceutical industry , quality (philosophy) , quality assurance , computer science , process (computing) , data validation , model validation , product (mathematics) , process analytical technology , verification and validation , risk analysis (engineering) , data science , engineering , work in process , medicine , operations management , mathematics , database , philosophy , external quality assessment , geometry , epistemology , pharmacology , operating system
Quality is the primordial intention of any industry and its products manufactured. Multiple views on obtaining such quality are the current interest in the pharmaceutical industry, and it has been maintained by validation. Validation is documented evidence that provides a high degree of assurance. Validation has become one of the pharmaceutical industries’ most recognized subjects. This article provides detailed information about pharmaceutical validation and its importance. Quality is always an imperative prerequisite when we consider the product. In this article, we discuss the types of validation, process validation, equipment validation, cleaning, and analytical method validation. Validation is the process that is used to confirm that the analytical procedure employed for a specific test is suitable for the intended use.
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