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Quantitative Analysis of Drugs in Pharmaceutical Formulations

PublisherCBS Publishers & Distributors
Author PD Sethi
Edition3rd Edition
Year2025
ISBN9788123905600
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Descriptions

Descriptions

Defensible with low limit of uncertainty and above all amenable to routine laboratory use and capable of being performed by personnel with minimum technical experience. Analytical methods for about 290 multi- component formulations in 18 chapters have been described with reasonable details to be reproduced without much difficulty, however, some degree of optimization and analytical skill may be required in certain cases. The methods for about 100 new formulations have been included while exhaustively revising- and up-dating the text. Methods which are obsolete have been deleted. Three additional chapters, i.e., Cardiac Drugs, Sedatives & Tranquillizers, and General Guidelines for Accreditation of Calibrating & Testing Laboratories with NABL, have been incorporated, the latter being extremely informative and useful for institutions seeking accreditation. Quality level of any analytical work primarily depends on the expertise of the analyst, based on the level of skill and practical experience attained; the analysts have been broadly grouped into five grades, enabling the quality control manager to assign analytical functions accordingly. Essential qualities of an analyst elaborated in the text should enable the analyst to evaluate his own performance periodically to maintain highest standards of analytical work.

Specifications

Specifications

ISBN9788123905600
Published Year2025
BindingHardcover with jacket
SubjectPharmaceutical Formulations
Pages672+16 colour plates
Weight0.4 (In Kg)
Dimension17 × 5 × 1.2
ReadershipBPharma & MPharma

About the Author

P

PD Sethi

P. D. Sethi obtained his B.Pharm. and M.Pharm. degrees from Panjab University, Chandigarh (India), and his Ph.D. from the University of Madras. Dr. Sethi has been associated with prestigious Federal Drug Testing Laboratories as a Pharmaceutical Analyst and has pursued his analytical career for over 20 years. He has been actively associated with the Indian Pharmacopoeia (1996) as a Member of the Working Group, as well as Chairman and Member of several subcommittees. He continues to serve the National Accreditation Board for Testing and Calibration Laboratories (NABL), Department of Science and Technology, Government of India, as an evaluator. He has to his credit several monographs in the field of Pharmaceutical Analysis, the latest being Application of HPTLC in Quantitative Analysis of Pharmaceutical Formulations, the first exhaustive compilation on the subject. Because of his professional competence and commitment, he is highly respected within the analytical community. “To develop new analytical methods, an analyst needs a certain degree of ingenuity.”
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