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Validation is one of the key elements to fulfill the requirement of current good manufacturing specifications (CGMP) and good laboratory specifications (GLP). Every pharmaceutical industry should efficiently carry out testing on source materials, in-process materials, finished containers, and excipients. Validation of analytical methods is thought to be a crucial prerequisite for testing such medicinal compounds. It is necessary to create an analytical technique for testing API, excipients, and finished goods. For the testing of API, excipient and final product, an analytical procedure should be developed. Such welldeveloped procedure should essential assure that it will consistently produce the intended and precise result with high degree of accuracy. Validation of the analytical method is required to obtain such a precise result.
Keywords:
Analytical method validation, CGMP, GLP.
Cite Article:
"A COMPREHENSIVE REVIEW ON ANALYTICAL METHOD VALIDATION", International Journal of Science & Engineering Development Research (www.ijrti.org), ISSN:2455-2631, Vol.8, Issue 6, page no.44 - 48, June-2023, Available :http://www.ijrti.org/papers/IJRTI2306009.pdf
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ISSN:
2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator